Canonical Allele Identifier: CA355866470

Gene: FGF12

Linked Data

• MyVariant Identifiers: chr3:g.192053230C>A (hg19) ; chr3:g.192335441C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192335441C>A , CM000665.2:g.192335441C>A	GRCh38
NC_000003.11:g.192053230C>A , CM000665.1:g.192053230C>A	GRCh37
NC_000003.10:g.193535924C>A	NCBI36
NG_051966.1:g.397159G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000454309.7:c.334G>T	ENSP00000413496.2:p.Gly112Cys
ENST00000682819.2:n.401G>T
ENST00000683451.2:c.148G>T	ENSP00000508366.1:p.Gly50Cys
ENST00000682572.1:n.336G>T
ENST00000682819.1:n.367G>T
ENST00000683451.1:c.148G>T	ENSP00000508366.1:p.Gly50Cys
ENST00000683935.1:c.148G>T	ENSP00000507098.1:p.Gly50Cys
ENST00000684282.1:c.76G>T	ENSP00000507149.1:p.Gly26Cys
ENST00000684728.1:c.76G>T	ENSP00000506839.1:p.Gly26Cys
ENST00000445105.7:c.148G>T MANE Select	ENSP00000393686.1:p.Gly50Cys
ENST00000418610.1:c.148G>T	ENSP00000395517.1:p.Gly50Cys
ENST00000430714.5:c.37G>T	ENSP00000410125.1:p.Gly13Cys
ENST00000445105.6:c.148G>T	ENSP00000393686.1:p.Gly50Cys
ENST00000448795.5:c.76G>T	ENSP00000412904.1:p.Gly26Cys
ENST00000450716.5:c.148G>T	ENSP00000397635.1:p.Gly50Cys
ENST00000454309.6:c.334G>T	ENSP00000413496.2:p.Gly112Cys
NM_004113.5:c.148G>T	NP_004104.3:p.Gly50Cys
NM_021032.4:c.334G>T	NP_066360.1:p.Gly112Cys
XM_005247227.1:c.226G>T	XP_005247284.1:p.Gly76Cys
XM_006713538.2:c.139G>T	XP_006713601.1:p.Gly47Cys
XM_006713539.2:c.76G>T	XP_006713602.1:p.Gly26Cys
XM_005247227.2:c.226G>T	XP_005247284.1:p.Gly76Cys
XM_006713538.3:c.139G>T	XP_006713601.1:p.Gly47Cys
XM_024453395.1:c.76G>T	XP_024309163.1:p.Gly26Cys
NM_001377292.1:c.37G>T	NP_001364221.1:p.Gly13Cys
NM_001377293.1:c.76G>T	NP_001364222.1:p.Gly26Cys
NM_001377294.1:c.76G>T	NP_001364223.1:p.Gly26Cys
NM_004113.6:c.148G>T MANE Select	NP_004104.3:p.Gly50Cys
NM_021032.5:c.334G>T	NP_066360.1:p.Gly112Cys