Canonical Allele Identifier: CA381087712

Gene: FERMT3

Linked Data

• gnomAD v4: 11-64220531-C-T
• MyVariant Identifiers: chr11:g.63988003C>T (hg19) ; chr11:g.64220531C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64220531C>T , CM000673.2:g.64220531C>T	GRCh38
NC_000011.9:g.63988003C>T , CM000673.1:g.63988003C>T	GRCh37
NC_000011.8:g.63744579C>T	NCBI36
NG_016360.1:g.18852C>T , LRG_180:g.18852C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279227.10:c.1419C>T	ENSP00000279227.5:p.Ile473=
ENST00000540554.2:n.2585C>T
ENST00000541252.2:c.867C>T	ENSP00000438885.2:p.Ile289=
ENST00000541326.6:n.828C>T
ENST00000544997.6:c.1407C>T	ENSP00000445778.2:p.Ile469=
ENST00000545896.2:c.96C>T	ENSP00000440209.2:p.Ile32=
ENST00000546255.2:n.1711C>T
ENST00000698845.1:c.*602C>T	ENSP00000513981.1:n.*602C>T
ENST00000698846.1:n.1653C>T
ENST00000698847.1:c.*812C>T	ENSP00000513982.1:n.*812C>T
ENST00000698849.1:n.527C>T
ENST00000698850.1:n.1175C>T
ENST00000698852.1:c.1407C>T	ENSP00000513984.1:p.Ile469=
ENST00000698853.1:c.*636C>T	ENSP00000513985.1:n.*636C>T
ENST00000698854.1:c.*737C>T	ENSP00000513986.1:n.*737C>T
ENST00000698855.1:n.3059C>T
ENST00000698856.1:n.2753C>T
ENST00000698859.1:n.1571C>T
ENST00000698860.1:c.1419C>T	ENSP00000513988.1:p.Ile473=
ENST00000698861.1:c.1407C>T	ENSP00000513989.1:p.Ile469=
ENST00000698862.1:c.*703C>T	ENSP00000513990.1:n.*703C>T
ENST00000698863.1:c.1407C>T	ENSP00000513991.1:p.Ile469=
ENST00000698864.1:n.1622C>T
ENST00000698865.1:c.1428C>T	ENSP00000513992.1:p.Ile476=
ENST00000698866.1:c.*921C>T	ENSP00000513993.1:n.*921C>T
ENST00000698867.1:n.5382C>T
ENST00000698868.1:c.1272C>T	ENSP00000513994.1:p.Ile424=
ENST00000698869.1:c.1311+205C>T	ENSP00000513995.1:n.1311+205C>T
ENST00000698870.1:c.1407C>T	ENSP00000513996.1:p.Ile469=
ENST00000698871.1:n.1930C>T
ENST00000698872.1:c.*196C>T	ENSP00000513997.1:n.*196C>T
ENST00000698873.1:c.*602C>T	ENSP00000513998.1:n.*602C>T
ENST00000698874.1:c.867C>T	ENSP00000513999.1:p.Ile289=
ENST00000698875.1:n.1267C>T
ENST00000698876.1:n.1455C>T
ENST00000698877.1:n.975C>T
ENST00000698878.1:c.1401C>T	ENSP00000514000.1:p.Ile467=
ENST00000698880.1:c.1275C>T
ENST00000345728.10:c.1407C>T MANE Select	ENSP00000339950.5:p.Ile469=
ENST00000279227.9:c.1419C>T	ENSP00000279227.5:p.Ile473=
ENST00000345728.9:c.1407C>T	ENSP00000339950.5:p.Ile469=
ENST00000541326.5:n.823C>T
ENST00000545896.1:c.95C>T	ENSP00000440209.1:p.Ser32Phe
NM_031471.5:c.1407C>T	NP_113659.3:p.Ile469=
NM_178443.2:c.1419C>T , LRG_180t1:c.1419C>T	NP_848537.1:p.Ile473=
XM_011545294.1:c.1419C>T	XP_011543596.1:p.Ile473=
XM_011545295.1:c.879C>T	XP_011543597.1:p.Ile293=
XM_011545296.1:c.879C>T	XP_011543598.1:p.Ile293=
XM_011545294.3:c.1419C>T	XP_011543596.1:p.Ile473=
XM_011545295.2:c.879C>T	XP_011543597.1:p.Ile293=
XM_017018398.2:c.1407C>T	XP_016873887.1:p.Ile469=
XM_017018399.1:c.867C>T	XP_016873888.1:p.Ile289=
NM_031471.6:c.1407C>T MANE Select	NP_113659.3:p.Ile469=
NM_001382361.1:c.1407C>T	NP_001369290.1:p.Ile469=
NM_001382362.1:c.1419C>T	NP_001369291.1:p.Ile473=
NM_001382363.1:c.867C>T	NP_001369292.1:p.Ile289=
NM_001382364.1:c.879C>T	NP_001369293.1:p.Ile293=
NM_001382448.1:c.1407C>T	NP_001369377.1:p.Ile469=
NM_178443.3:c.1419C>T	NP_848537.1:p.Ile473=