Canonical Allele Identifier: CA90387571

Gene: FGF12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192170471C>T , CM000665.2:g.192170471C>T	GRCh38
NC_000003.11:g.191888260C>T , CM000665.1:g.191888260C>T	GRCh37
NC_000003.10:g.193370954C>T	NCBI36
NG_051966.1:g.562129G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454309.7:c.600G>A	ENSP00000413496.2:p.Pro200=
ENST00000683451.2:c.414G>A	ENSP00000508366.1:p.Pro138=
ENST00000682572.1:n.417-26344G>A
ENST00000683451.1:c.414G>A	ENSP00000508366.1:p.Pro138=
ENST00000683935.1:c.414G>A	ENSP00000507098.1:p.Pro138=
ENST00000684282.1:c.342G>A	ENSP00000507149.1:p.Pro114=
ENST00000684728.1:c.342G>A	ENSP00000506839.1:p.Pro114=
ENST00000445105.7:c.414G>A MANE Select	ENSP00000393686.1:p.Pro138=
ENST00000430714.5:c.303G>A	ENSP00000410125.1:p.Pro101=
ENST00000440901.4:n.285G>A
ENST00000445105.6:c.414G>A	ENSP00000393686.1:p.Pro138=
ENST00000448795.5:c.342G>A	ENSP00000412904.1:p.Pro114=
ENST00000450716.5:c.414G>A	ENSP00000397635.1:p.Pro138=
ENST00000454309.6:c.600G>A	ENSP00000413496.2:p.Pro200=
NM_004113.5:c.414G>A	NP_004104.3:p.Pro138=
NM_021032.4:c.600G>A	NP_066360.1:p.Pro200=
XM_005247227.1:c.492G>A	XP_005247284.1:p.Pro164=
XM_006713538.2:c.405G>A	XP_006713601.1:p.Pro135=
XM_006713539.2:c.342G>A	XP_006713602.1:p.Pro114=
XM_005247227.2:c.492G>A	XP_005247284.1:p.Pro164=
XM_006713538.3:c.405G>A	XP_006713601.1:p.Pro135=
XM_024453395.1:c.342G>A	XP_024309163.1:p.Pro114=
NM_001377292.1:c.303G>A	NP_001364221.1:p.Pro101=
NM_001377293.1:c.342G>A	NP_001364222.1:p.Pro114=
NM_001377294.1:c.342G>A	NP_001364223.1:p.Pro114=
NM_004113.6:c.414G>A MANE Select	NP_004104.3:p.Pro138=
NM_021032.5:c.600G>A	NP_066360.1:p.Pro200=