Canonical Allele Identifier: CA475151739

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987753G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220281G>C , CM000673.2:g.64220281G>C	GRCh38
NC_000011.9:g.63987753G>C , CM000673.1:g.63987753G>C	GRCh37
NC_000011.8:g.63744329G>C	NCBI36
NG_016360.1:g.18602G>C , LRG_180:g.18602G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1278G>C	ENSP00000279227.5:p.Val426=
ENST00000540554.2:n.2335G>C
ENST00000541252.2:c.726G>C	ENSP00000438885.2:p.Val242=
ENST00000541326.6:n.578G>C
ENST00000544997.6:c.1266G>C	ENSP00000445778.2:p.Val422=
ENST00000546255.2:n.1461G>C
ENST00000698845.1:c.*461G>C	ENSP00000513981.1:n.*461G>C
ENST00000698846.1:n.1403G>C
ENST00000698847.1:c.*671G>C	ENSP00000513982.1:n.*671G>C
ENST00000698848.1:n.455G>C
ENST00000698849.1:n.386G>C
ENST00000698850.1:n.925G>C
ENST00000698852.1:c.1266G>C	ENSP00000513984.1:p.Val422=
ENST00000698853.1:c.*495G>C	ENSP00000513985.1:n.*495G>C
ENST00000698854.1:c.*596G>C	ENSP00000513986.1:n.*596G>C
ENST00000698855.1:n.2918G>C
ENST00000698856.1:n.2503G>C
ENST00000698859.1:n.1430G>C
ENST00000698860.1:c.1278G>C	ENSP00000513988.1:p.Val426=
ENST00000698861.1:c.1266G>C	ENSP00000513989.1:p.Val422=
ENST00000698862.1:c.*562G>C	ENSP00000513990.1:n.*562G>C
ENST00000698863.1:c.1266G>C	ENSP00000513991.1:p.Val422=
ENST00000698864.1:n.1372G>C
ENST00000698865.1:c.1287G>C	ENSP00000513992.1:p.Val429=
ENST00000698866.1:c.*671G>C	ENSP00000513993.1:n.*671G>C
ENST00000698867.1:n.5241G>C
ENST00000698868.1:c.1131G>C	ENSP00000513994.1:p.Val377=
ENST00000698869.1:c.1266G>C	ENSP00000513995.1:p.Val422=
ENST00000698870.1:c.1266G>C	ENSP00000513996.1:p.Val422=
ENST00000698871.1:n.1789G>C
ENST00000698872.1:c.*55G>C	ENSP00000513997.1:n.*55G>C
ENST00000698873.1:c.*461G>C	ENSP00000513998.1:n.*461G>C
ENST00000698874.1:c.726G>C	ENSP00000513999.1:p.Val242=
ENST00000698875.1:n.1126G>C
ENST00000698876.1:n.1205G>C
ENST00000698877.1:n.834G>C
ENST00000698878.1:c.1266G>C	ENSP00000514000.1:p.Val422=
ENST00000698880.1:c.1106G>C
ENST00000345728.10:c.1266G>C MANE Select	ENSP00000339950.5:p.Val422=
ENST00000279227.9:c.1278G>C	ENSP00000279227.5:p.Val426=
ENST00000345728.9:c.1266G>C	ENSP00000339950.5:p.Val422=
ENST00000540957.1:n.419G>C
ENST00000541326.5:n.573G>C
NM_031471.5:c.1266G>C	NP_113659.3:p.Val422=
NM_178443.2:c.1278G>C , LRG_180t1:c.1278G>C	NP_848537.1:p.Val426=
XM_011545294.1:c.1278G>C	XP_011543596.1:p.Val426=
XM_011545295.1:c.738G>C	XP_011543597.1:p.Val246=
XM_011545296.1:c.738G>C	XP_011543598.1:p.Val246=
XM_011545294.3:c.1278G>C	XP_011543596.1:p.Val426=
XM_011545295.2:c.738G>C	XP_011543597.1:p.Val246=
XM_017018398.2:c.1266G>C	XP_016873887.1:p.Val422=
XM_017018399.1:c.726G>C	XP_016873888.1:p.Val242=
NM_031471.6:c.1266G>C MANE Select	NP_113659.3:p.Val422=
NM_001382361.1:c.1266G>C	NP_001369290.1:p.Val422=
NM_001382362.1:c.1278G>C	NP_001369291.1:p.Val426=
NM_001382363.1:c.726G>C	NP_001369292.1:p.Val242=
NM_001382364.1:c.738G>C	NP_001369293.1:p.Val246=
NM_001382448.1:c.1266G>C	NP_001369377.1:p.Val422=
NM_178443.3:c.1278G>C	NP_848537.1:p.Val426=