Canonical Allele Identifier: CA1978638872

Gene: FERMT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220459_64220469delinsGGCTGGCTGCC , CM000673.2:g.64220459_64220469delinsGGCTGGCTGCC	GRCh38
NC_000011.9:g.63987931_63987941delinsGGCTGGCTGCC , CM000673.1:g.63987931_63987941delinsGGCTGGCTGCC	GRCh37
NC_000011.8:g.63744507_63744517delinsGGCTGGCTGCC	NCBI36
NG_016360.1:g.18780_18790delinsGGCTGGCTGCC , LRG_180:g.18780_18790delinsGGCTGGCTGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1347_1357delinsGGCTGGCTGCC	ENSP00000279227.5:p.Met449=
ENST00000540554.2:n.2513_2523delinsGGCTGGCTGCC
ENST00000541252.2:c.795_805delinsGGCTGGCTGCC	ENSP00000438885.2:p.Met265=
ENST00000541326.6:n.756_766delinsGGCTGGCTGCC
ENST00000544997.6:c.1335_1345delinsGGCTGGCTGCC	ENSP00000445778.2:p.Met445=
ENST00000545896.2:c.24_34delinsGGCTGGCTGCC	ENSP00000440209.2:p.Met8=
ENST00000546255.2:n.1639_1649delinsGGCTGGCTGCC
ENST00000698845.1:c.*530_*540delinsGGCTGGCTGCC	ENSP00000513981.1:n.*530_*540delinsGGCTGGCTGCC
ENST00000698846.1:n.1581_1591delinsGGCTGGCTGCC
ENST00000698847.1:c.*740_*750delinsGGCTGGCTGCC	ENSP00000513982.1:n.*740_*750delinsGGCTGGCTGCC
ENST00000698848.1:n.633_643delinsGGCTGGCTGCC
ENST00000698849.1:n.455_465delinsGGCTGGCTGCC
ENST00000698850.1:n.1103_1113delinsGGCTGGCTGCC
ENST00000698852.1:c.1335_1345delinsGGCTGGCTGCC	ENSP00000513984.1:p.Met445=
ENST00000698853.1:c.*564_*574delinsGGCTGGCTGCC	ENSP00000513985.1:n.*564_*574delinsGGCTGGCTGCC
ENST00000698854.1:c.*665_*675delinsGGCTGGCTGCC	ENSP00000513986.1:n.*665_*675delinsGGCTGGCTGCC
ENST00000698855.1:n.2987_2997delinsGGCTGGCTGCC
ENST00000698856.1:n.2681_2691delinsGGCTGGCTGCC
ENST00000698859.1:n.1499_1509delinsGGCTGGCTGCC
ENST00000698860.1:c.1347_1357delinsGGCTGGCTGCC	ENSP00000513988.1:p.Met449=
ENST00000698861.1:c.1335_1345delinsGGCTGGCTGCC	ENSP00000513989.1:p.Met445=
ENST00000698862.1:c.*631_*641delinsGGCTGGCTGCC	ENSP00000513990.1:n.*631_*641delinsGGCTGGCTGCC
ENST00000698863.1:c.1335_1345delinsGGCTGGCTGCC	ENSP00000513991.1:p.Met445=
ENST00000698864.1:n.1550_1560delinsGGCTGGCTGCC
ENST00000698865.1:c.1356_1366delinsGGCTGGCTGCC	ENSP00000513992.1:p.Met452=
ENST00000698866.1:c.*849_*859delinsGGCTGGCTGCC	ENSP00000513993.1:n.*849_*859delinsGGCTGGCTGCC
ENST00000698867.1:n.5310_5320delinsGGCTGGCTGCC
ENST00000698868.1:c.1200_1210delinsGGCTGGCTGCC	ENSP00000513994.1:p.Met400=
ENST00000698869.1:c.1311+133_1311+143delinsGGCTGGCTGCC	ENSP00000513995.1:n.1311+133_1311+143delinsGGCTGGCTGCC
ENST00000698870.1:c.1335_1345delinsGGCTGGCTGCC	ENSP00000513996.1:p.Met445=
ENST00000698871.1:n.1858_1868delinsGGCTGGCTGCC
ENST00000698872.1:c.*124_*134delinsGGCTGGCTGCC	ENSP00000513997.1:n.*124_*134delinsGGCTGGCTGCC
ENST00000698873.1:c.*530_*540delinsGGCTGGCTGCC	ENSP00000513998.1:n.*530_*540delinsGGCTGGCTGCC
ENST00000698874.1:c.795_805delinsGGCTGGCTGCC	ENSP00000513999.1:p.Met265=
ENST00000698875.1:n.1195_1205delinsGGCTGGCTGCC
ENST00000698876.1:n.1383_1393delinsGGCTGGCTGCC
ENST00000698877.1:n.903_913delinsGGCTGGCTGCC
ENST00000698878.1:c.1329_1339delinsGGCTGGCTGCC	ENSP00000514000.1:p.Met443=
ENST00000698880.1:c.1203_1213delinsGGCTGGCTGCC
ENST00000345728.10:c.1335_1345delinsGGCTGGCTGCC MANE Select	ENSP00000339950.5:p.Met445=
ENST00000279227.9:c.1347_1357delinsGGCTGGCTGCC	ENSP00000279227.5:p.Met449=
ENST00000345728.9:c.1335_1345delinsGGCTGGCTGCC	ENSP00000339950.5:p.Met445=
ENST00000541326.5:n.751_761delinsGGCTGGCTGCC
ENST00000545896.1:c.23_33delinsGGCTGGCTGCC	ENSP00000440209.1:p.Trp8=
NM_031471.5:c.1335_1345delinsGGCTGGCTGCC	NP_113659.3:p.Met445=
NM_178443.2:c.1347_1357delinsGGCTGGCTGCC , LRG_180t1:c.1347_1357delinsGGCTGGCTGCC	NP_848537.1:p.Met449=
XM_011545294.1:c.1347_1357delinsGGCTGGCTGCC	XP_011543596.1:p.Met449=
XM_011545295.1:c.807_817delinsGGCTGGCTGCC	XP_011543597.1:p.Met269=
XM_011545296.1:c.807_817delinsGGCTGGCTGCC	XP_011543598.1:p.Met269=
XM_011545294.3:c.1347_1357delinsGGCTGGCTGCC	XP_011543596.1:p.Met449=
XM_011545295.2:c.807_817delinsGGCTGGCTGCC	XP_011543597.1:p.Met269=
XM_017018398.2:c.1335_1345delinsGGCTGGCTGCC	XP_016873887.1:p.Met445=
XM_017018399.1:c.795_805delinsGGCTGGCTGCC	XP_016873888.1:p.Met265=
NM_031471.6:c.1335_1345delinsGGCTGGCTGCC MANE Select	NP_113659.3:p.Met445=
NM_001382361.1:c.1335_1345delinsGGCTGGCTGCC	NP_001369290.1:p.Met445=
NM_001382362.1:c.1347_1357delinsGGCTGGCTGCC	NP_001369291.1:p.Met449=
NM_001382363.1:c.795_805delinsGGCTGGCTGCC	NP_001369292.1:p.Met265=
NM_001382364.1:c.807_817delinsGGCTGGCTGCC	NP_001369293.1:p.Met269=
NM_001382448.1:c.1335_1345delinsGGCTGGCTGCC	NP_001369377.1:p.Met445=
NM_178443.3:c.1347_1357delinsGGCTGGCTGCC	NP_848537.1:p.Met449=