Canonical Allele Identifier: CA355866474

Gene: FGF12

Linked Data

• MyVariant Identifiers: chr3:g.192053232A>G (hg19) ; chr3:g.192335443A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192335443A>G , CM000665.2:g.192335443A>G	GRCh38
NC_000003.11:g.192053232A>G , CM000665.1:g.192053232A>G	GRCh37
NC_000003.10:g.193535926A>G	NCBI36
NG_051966.1:g.397157T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000454309.7:c.332T>C	ENSP00000413496.2:p.Val111Ala
ENST00000682819.2:n.399T>C
ENST00000683451.2:c.146T>C	ENSP00000508366.1:p.Val49Ala
ENST00000682572.1:n.334T>C
ENST00000682819.1:n.365T>C
ENST00000683451.1:c.146T>C	ENSP00000508366.1:p.Val49Ala
ENST00000683935.1:c.146T>C	ENSP00000507098.1:p.Val49Ala
ENST00000684282.1:c.74T>C	ENSP00000507149.1:p.Val25Ala
ENST00000684728.1:c.74T>C	ENSP00000506839.1:p.Val25Ala
ENST00000445105.7:c.146T>C MANE Select	ENSP00000393686.1:p.Val49Ala
ENST00000418610.1:c.146T>C	ENSP00000395517.1:p.Val49Ala
ENST00000430714.5:c.35T>C	ENSP00000410125.1:p.Val12Ala
ENST00000445105.6:c.146T>C	ENSP00000393686.1:p.Val49Ala
ENST00000448795.5:c.74T>C	ENSP00000412904.1:p.Val25Ala
ENST00000450716.5:c.146T>C	ENSP00000397635.1:p.Val49Ala
ENST00000454309.6:c.332T>C	ENSP00000413496.2:p.Val111Ala
NM_004113.5:c.146T>C	NP_004104.3:p.Val49Ala
NM_021032.4:c.332T>C	NP_066360.1:p.Val111Ala
XM_005247227.1:c.224T>C	XP_005247284.1:p.Val75Ala
XM_006713538.2:c.137T>C	XP_006713601.1:p.Val46Ala
XM_006713539.2:c.74T>C	XP_006713602.1:p.Val25Ala
XM_005247227.2:c.224T>C	XP_005247284.1:p.Val75Ala
XM_006713538.3:c.137T>C	XP_006713601.1:p.Val46Ala
XM_024453395.1:c.74T>C	XP_024309163.1:p.Val25Ala
NM_001377292.1:c.35T>C	NP_001364221.1:p.Val12Ala
NM_001377293.1:c.74T>C	NP_001364222.1:p.Val25Ala
NM_001377294.1:c.74T>C	NP_001364223.1:p.Val25Ala
NM_004113.6:c.146T>C MANE Select	NP_004104.3:p.Val49Ala
NM_021032.5:c.332T>C	NP_066360.1:p.Val111Ala