Canonical Allele Identifier: CA381087575

Gene: FERMT3

Linked Data

• MyVariant Identifiers: chr11:g.63987971G>T (hg19) ; chr11:g.64220499G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220499G>T , CM000673.2:g.64220499G>T	GRCh38
NC_000011.9:g.63987971G>T , CM000673.1:g.63987971G>T	GRCh37
NC_000011.8:g.63744547G>T	NCBI36
NG_016360.1:g.18820G>T , LRG_180:g.18820G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1387G>T	ENSP00000279227.5:p.Asp463Tyr
ENST00000540554.2:n.2553G>T
ENST00000541252.2:c.835G>T	ENSP00000438885.2:p.Asp279Tyr
ENST00000541326.6:n.796G>T
ENST00000544997.6:c.1375G>T	ENSP00000445778.2:p.Asp459Tyr
ENST00000545896.2:c.64G>T	ENSP00000440209.2:p.Asp22Tyr
ENST00000546255.2:n.1679G>T
ENST00000698845.1:c.*570G>T	ENSP00000513981.1:n.*570G>T
ENST00000698846.1:n.1621G>T
ENST00000698847.1:c.*780G>T	ENSP00000513982.1:n.*780G>T
ENST00000698849.1:n.495G>T
ENST00000698850.1:n.1143G>T
ENST00000698852.1:c.1375G>T	ENSP00000513984.1:p.Asp459Tyr
ENST00000698853.1:c.*604G>T	ENSP00000513985.1:n.*604G>T
ENST00000698854.1:c.*705G>T	ENSP00000513986.1:n.*705G>T
ENST00000698855.1:n.3027G>T
ENST00000698856.1:n.2721G>T
ENST00000698859.1:n.1539G>T
ENST00000698860.1:c.1387G>T	ENSP00000513988.1:p.Asp463Tyr
ENST00000698861.1:c.1375G>T	ENSP00000513989.1:p.Asp459Tyr
ENST00000698862.1:c.*671G>T	ENSP00000513990.1:n.*671G>T
ENST00000698863.1:c.1375G>T	ENSP00000513991.1:p.Asp459Tyr
ENST00000698864.1:n.1590G>T
ENST00000698865.1:c.1396G>T	ENSP00000513992.1:p.Asp466Tyr
ENST00000698866.1:c.*889G>T	ENSP00000513993.1:n.*889G>T
ENST00000698867.1:n.5350G>T
ENST00000698868.1:c.1240G>T	ENSP00000513994.1:p.Asp414Tyr
ENST00000698869.1:c.1311+173G>T	ENSP00000513995.1:n.1311+173G>T
ENST00000698870.1:c.1375G>T	ENSP00000513996.1:p.Asp459Tyr
ENST00000698871.1:n.1898G>T
ENST00000698872.1:c.*164G>T	ENSP00000513997.1:n.*164G>T
ENST00000698873.1:c.*570G>T	ENSP00000513998.1:n.*570G>T
ENST00000698874.1:c.835G>T	ENSP00000513999.1:p.Asp279Tyr
ENST00000698875.1:n.1235G>T
ENST00000698876.1:n.1423G>T
ENST00000698877.1:n.943G>T
ENST00000698878.1:c.1369G>T	ENSP00000514000.1:p.Asp457Tyr
ENST00000698880.1:c.1243G>T
ENST00000345728.10:c.1375G>T MANE Select	ENSP00000339950.5:p.Asp459Tyr
ENST00000279227.9:c.1387G>T	ENSP00000279227.5:p.Asp463Tyr
ENST00000345728.9:c.1375G>T	ENSP00000339950.5:p.Asp459Tyr
ENST00000541326.5:n.791G>T
ENST00000545896.1:c.63G>T	ENSP00000440209.1:p.Pro21=
NM_031471.5:c.1375G>T	NP_113659.3:p.Asp459Tyr
NM_178443.2:c.1387G>T , LRG_180t1:c.1387G>T	NP_848537.1:p.Asp463Tyr
XM_011545294.1:c.1387G>T	XP_011543596.1:p.Asp463Tyr
XM_011545295.1:c.847G>T	XP_011543597.1:p.Asp283Tyr
XM_011545296.1:c.847G>T	XP_011543598.1:p.Asp283Tyr
XM_011545294.3:c.1387G>T	XP_011543596.1:p.Asp463Tyr
XM_011545295.2:c.847G>T	XP_011543597.1:p.Asp283Tyr
XM_017018398.2:c.1375G>T	XP_016873887.1:p.Asp459Tyr
XM_017018399.1:c.835G>T	XP_016873888.1:p.Asp279Tyr
NM_031471.6:c.1375G>T MANE Select	NP_113659.3:p.Asp459Tyr
NM_001382361.1:c.1375G>T	NP_001369290.1:p.Asp459Tyr
NM_001382362.1:c.1387G>T	NP_001369291.1:p.Asp463Tyr
NM_001382363.1:c.835G>T	NP_001369292.1:p.Asp279Tyr
NM_001382364.1:c.847G>T	NP_001369293.1:p.Asp283Tyr
NM_001382448.1:c.1375G>T	NP_001369377.1:p.Asp459Tyr
NM_178443.3:c.1387G>T	NP_848537.1:p.Asp463Tyr