Canonical Allele Identifier: CA2755800

Gene: FGF12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192335425G>A , CM000665.2:g.192335425G>A	GRCh38
NC_000003.11:g.192053214G>A , CM000665.1:g.192053214G>A	GRCh37
NC_000003.10:g.193535908G>A	NCBI36
NG_051966.1:g.397175C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454309.7:c.350C>T	ENSP00000413496.2:p.Ala117Val
ENST00000682819.2:n.417C>T
ENST00000683451.2:c.164C>T	ENSP00000508366.1:p.Ala55Val
ENST00000682572.1:n.352C>T
ENST00000682819.1:n.383C>T
ENST00000683451.1:c.164C>T	ENSP00000508366.1:p.Ala55Val
ENST00000683935.1:c.164C>T	ENSP00000507098.1:p.Ala55Val
ENST00000684282.1:c.92C>T	ENSP00000507149.1:p.Ala31Val
ENST00000684728.1:c.92C>T	ENSP00000506839.1:p.Ala31Val
ENST00000445105.7:c.164C>T MANE Select	ENSP00000393686.1:p.Ala55Val
ENST00000418610.1:c.164C>T	ENSP00000395517.1:p.Ala55Val
ENST00000430714.5:c.53C>T	ENSP00000410125.1:p.Ala18Val
ENST00000445105.6:c.164C>T	ENSP00000393686.1:p.Ala55Val
ENST00000448795.5:c.92C>T	ENSP00000412904.1:p.Ala31Val
ENST00000450716.5:c.164C>T	ENSP00000397635.1:p.Ala55Val
ENST00000454309.6:c.350C>T	ENSP00000413496.2:p.Ala117Val
NM_004113.5:c.164C>T	NP_004104.3:p.Ala55Val
NM_021032.4:c.350C>T	NP_066360.1:p.Ala117Val
XM_005247227.1:c.242C>T	XP_005247284.1:p.Ala81Val
XM_006713538.2:c.155C>T	XP_006713601.1:p.Ala52Val
XM_006713539.2:c.92C>T	XP_006713602.1:p.Ala31Val
XM_005247227.2:c.242C>T	XP_005247284.1:p.Ala81Val
XM_006713538.3:c.155C>T	XP_006713601.1:p.Ala52Val
XM_024453395.1:c.92C>T	XP_024309163.1:p.Ala31Val
NM_001377292.1:c.53C>T	NP_001364221.1:p.Ala18Val
NM_001377293.1:c.92C>T	NP_001364222.1:p.Ala31Val
NM_001377294.1:c.92C>T	NP_001364223.1:p.Ala31Val
NM_004113.6:c.164C>T MANE Select	NP_004104.3:p.Ala55Val
NM_021032.5:c.350C>T	NP_066360.1:p.Ala117Val