Canonical Allele Identifier: CA2755842

Gene: FGF12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192360463G>T , CM000665.2:g.192360463G>T	GRCh38
NC_000003.11:g.192078252G>T , CM000665.1:g.192078252G>T	GRCh37
NC_000003.10:g.193560946G>T	NCBI36
NG_051966.1:g.372137C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454309.7:c.275C>A	ENSP00000413496.2:p.Thr92Asn
ENST00000682819.2:n.342C>A
ENST00000683451.2:c.89C>A	ENSP00000508366.1:p.Thr30Asn
ENST00000682572.1:n.277C>A
ENST00000682819.1:n.308C>A
ENST00000683451.1:c.89C>A	ENSP00000508366.1:p.Thr30Asn
ENST00000683935.1:c.89C>A	ENSP00000507098.1:p.Thr30Asn
ENST00000684282.1:c.17C>A	ENSP00000507149.1:p.Thr6Asn
ENST00000684728.1:c.17C>A	ENSP00000506839.1:p.Thr6Asn
ENST00000445105.7:c.89C>A MANE Select	ENSP00000393686.1:p.Thr30Asn
ENST00000418610.1:c.89C>A	ENSP00000395517.1:p.Thr30Asn
ENST00000430714.5:c.14-24999C>A	ENSP00000410125.1:n.14-24999C>A
ENST00000445105.6:c.89C>A	ENSP00000393686.1:p.Thr30Asn
ENST00000448795.5:c.17C>A	ENSP00000412904.1:p.Thr6Asn
ENST00000450716.5:c.89C>A	ENSP00000397635.1:p.Thr30Asn
ENST00000454309.6:c.275C>A	ENSP00000413496.2:p.Thr92Asn
NM_004113.5:c.89C>A	NP_004104.3:p.Thr30Asn
NM_021032.4:c.275C>A	NP_066360.1:p.Thr92Asn
XM_005247227.1:c.167C>A	XP_005247284.1:p.Thr56Asn
XM_006713538.2:c.80C>A	XP_006713601.1:p.Thr27Asn
XM_006713539.2:c.17C>A	XP_006713602.1:p.Thr6Asn
XM_005247227.2:c.167C>A	XP_005247284.1:p.Thr56Asn
XM_006713538.3:c.80C>A	XP_006713601.1:p.Thr27Asn
XM_024453395.1:c.17C>A	XP_024309163.1:p.Thr6Asn
NM_001377292.1:c.14-24999C>A	NP_001364221.1:n.14-24999C>A
NM_001377293.1:c.17C>A	NP_001364222.1:p.Thr6Asn
NM_001377294.1:c.17C>A	NP_001364223.1:p.Thr6Asn
NM_004113.6:c.89C>A MANE Select	NP_004104.3:p.Thr30Asn
NM_021032.5:c.275C>A	NP_066360.1:p.Thr92Asn