Canonical Allele Identifier: CA355866273

Gene: FGF12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192170653C>T , CM000665.2:g.192170653C>T	GRCh38
NC_000003.11:g.191888442C>T , CM000665.1:g.191888442C>T	GRCh37
NC_000003.10:g.193371136C>T	NCBI36
NG_051966.1:g.561947G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454309.7:c.418G>A	ENSP00000413496.2:p.Val140Ile
ENST00000683451.2:c.232G>A	ENSP00000508366.1:p.Val78Ile
ENST00000682572.1:n.417-26526G>A
ENST00000683451.1:c.232G>A	ENSP00000508366.1:p.Val78Ile
ENST00000683935.1:c.232G>A	ENSP00000507098.1:p.Val78Ile
ENST00000684282.1:c.160G>A	ENSP00000507149.1:p.Val54Ile
ENST00000684728.1:c.160G>A	ENSP00000506839.1:p.Val54Ile
ENST00000445105.7:c.232G>A MANE Select	ENSP00000393686.1:p.Val78Ile
ENST00000418610.1:c.232G>A	ENSP00000395517.1:p.Val78Ile
ENST00000430714.5:c.121G>A	ENSP00000410125.1:p.Val41Ile
ENST00000440901.4:n.103G>A
ENST00000445105.6:c.232G>A	ENSP00000393686.1:p.Val78Ile
ENST00000448795.5:c.160G>A	ENSP00000412904.1:p.Val54Ile
ENST00000450716.5:c.232G>A	ENSP00000397635.1:p.Val78Ile
ENST00000454309.6:c.418G>A	ENSP00000413496.2:p.Val140Ile
NM_004113.5:c.232G>A	NP_004104.3:p.Val78Ile
NM_021032.4:c.418G>A	NP_066360.1:p.Val140Ile
XM_005247227.1:c.310G>A	XP_005247284.1:p.Val104Ile
XM_006713538.2:c.223G>A	XP_006713601.1:p.Val75Ile
XM_006713539.2:c.160G>A	XP_006713602.1:p.Val54Ile
XM_005247227.2:c.310G>A	XP_005247284.1:p.Val104Ile
XM_006713538.3:c.223G>A	XP_006713601.1:p.Val75Ile
XM_024453395.1:c.160G>A	XP_024309163.1:p.Val54Ile
NM_001377292.1:c.121G>A	NP_001364221.1:p.Val41Ile
NM_001377293.1:c.160G>A	NP_001364222.1:p.Val54Ile
NM_001377294.1:c.160G>A	NP_001364223.1:p.Val54Ile
NM_004113.6:c.232G>A MANE Select	NP_004104.3:p.Val78Ile
NM_021032.5:c.418G>A	NP_066360.1:p.Val140Ile