Canonical Allele Identifier: CA437589000

Gene: FGF12

Linked Data

• MyVariant Identifiers: chr3:g.192053234G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192335445G>T , CM000665.2:g.192335445G>T	GRCh38
NC_000003.11:g.192053234G>T , CM000665.1:g.192053234G>T	GRCh37
NC_000003.10:g.193535928G>T	NCBI36
NG_051966.1:g.397155C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454309.7:c.330C>A	ENSP00000413496.2:p.Pro110=
ENST00000682819.2:n.397C>A
ENST00000683451.2:c.144C>A	ENSP00000508366.1:p.Pro48=
ENST00000682572.1:n.332C>A
ENST00000682819.1:n.363C>A
ENST00000683451.1:c.144C>A	ENSP00000508366.1:p.Pro48=
ENST00000683935.1:c.144C>A	ENSP00000507098.1:p.Pro48=
ENST00000684282.1:c.72C>A	ENSP00000507149.1:p.Pro24=
ENST00000684728.1:c.72C>A	ENSP00000506839.1:p.Pro24=
ENST00000445105.7:c.144C>A MANE Select	ENSP00000393686.1:p.Pro48=
ENST00000418610.1:c.144C>A	ENSP00000395517.1:p.Pro48=
ENST00000430714.5:c.33C>A	ENSP00000410125.1:p.Pro11=
ENST00000445105.6:c.144C>A	ENSP00000393686.1:p.Pro48=
ENST00000448795.5:c.72C>A	ENSP00000412904.1:p.Pro24=
ENST00000450716.5:c.144C>A	ENSP00000397635.1:p.Pro48=
ENST00000454309.6:c.330C>A	ENSP00000413496.2:p.Pro110=
NM_004113.5:c.144C>A	NP_004104.3:p.Pro48=
NM_021032.4:c.330C>A	NP_066360.1:p.Pro110=
XM_005247227.1:c.222C>A	XP_005247284.1:p.Pro74=
XM_006713538.2:c.135C>A	XP_006713601.1:p.Pro45=
XM_006713539.2:c.72C>A	XP_006713602.1:p.Pro24=
XM_005247227.2:c.222C>A	XP_005247284.1:p.Pro74=
XM_006713538.3:c.135C>A	XP_006713601.1:p.Pro45=
XM_024453395.1:c.72C>A	XP_024309163.1:p.Pro24=
NM_001377292.1:c.33C>A	NP_001364221.1:p.Pro11=
NM_001377293.1:c.72C>A	NP_001364222.1:p.Pro24=
NM_001377294.1:c.72C>A	NP_001364223.1:p.Pro24=
NM_004113.6:c.144C>A MANE Select	NP_004104.3:p.Pro48=
NM_021032.5:c.330C>A	NP_066360.1:p.Pro110=