Canonical Allele Identifier: CA1429671980

Gene: FGF12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192362043G= , CM000665.2:g.192362043G=	GRCh38
NC_000003.11:g.192079832G= , CM000665.1:g.192079832G=	GRCh37
NC_000003.10:g.193562526G=	NCBI36
NG_051966.1:g.370557C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454309.7:c.200-1505C=	ENSP00000413496.2:n.200-1505C=
ENST00000682819.2:n.267-1505C=
ENST00000683451.2:c.14-1505C=	ENSP00000508366.1:n.14-1505C=
ENST00000682572.1:n.202-1505C=
ENST00000682819.1:n.233-1505C=
ENST00000683451.1:c.14-1505C=	ENSP00000508366.1:n.14-1505C=
ENST00000683935.1:c.14-1505C=	ENSP00000507098.1:n.14-1505C=
ENST00000684282.1:c.-59-1505C=	ENSP00000507149.1:n.-59-1505C=
ENST00000684728.1:c.-59-1505C=	ENSP00000506839.1:n.-59-1505C=
ENST00000445105.7:c.14-1505C= MANE Select	ENSP00000393686.1:n.14-1505C=
ENST00000418610.1:c.14-1505C=	ENSP00000395517.1:n.14-1505C=
ENST00000430714.5:c.14-26579C=	ENSP00000410125.1:n.14-26579C=
ENST00000445105.6:c.14-1505C=	ENSP00000393686.1:n.14-1505C=
ENST00000448795.5:c.-59-1505C=	ENSP00000412904.1:n.-59-1505C=
ENST00000450716.5:c.14-1505C=	ENSP00000397635.1:n.14-1505C=
ENST00000454309.6:c.200-1505C=	ENSP00000413496.2:n.200-1505C=
NM_004113.5:c.14-1505C=	NP_004104.3:n.14-1505C=
NM_021032.4:c.200-1505C=	NP_066360.1:n.200-1505C=
XM_005247227.1:c.92-1505C=	XP_005247284.1:n.92-1505C=
XM_006713538.2:c.5-1505C=	XP_006713601.1:n.5-1505C=
XM_006713539.2:c.-59-1505C=	XP_006713602.1:n.-59-1505C=
XM_005247227.2:c.92-1505C=	XP_005247284.1:n.92-1505C=
XM_006713538.3:c.5-1505C=	XP_006713601.1:n.5-1505C=
XM_024453395.1:c.-59-1505C=	XP_024309163.1:n.-59-1505C=
NM_001377292.1:c.14-26579C=	NP_001364221.1:n.14-26579C=
NM_001377293.1:c.-59-1505C=	NP_001364222.1:n.-59-1505C=
NM_001377294.1:c.-59-1505C=	NP_001364223.1:n.-59-1505C=
NM_004113.6:c.14-1505C= MANE Select	NP_004104.3:n.14-1505C=
NM_021032.5:c.200-1505C=	NP_066360.1:n.200-1505C=