Canonical Allele Identifier: CA2755744

Gene: FGF12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192170586G>A , CM000665.2:g.192170586G>A	GRCh38
NC_000003.11:g.191888375G>A , CM000665.1:g.191888375G>A	GRCh37
NC_000003.10:g.193371069G>A	NCBI36
NG_051966.1:g.562014C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454309.7:c.485C>T	ENSP00000413496.2:p.Thr162Ile
ENST00000683451.2:c.299C>T	ENSP00000508366.1:p.Thr100Ile
ENST00000682572.1:n.417-26459C>T
ENST00000683451.1:c.299C>T	ENSP00000508366.1:p.Thr100Ile
ENST00000683935.1:c.299C>T	ENSP00000507098.1:p.Thr100Ile
ENST00000684282.1:c.227C>T	ENSP00000507149.1:p.Thr76Ile
ENST00000684728.1:c.227C>T	ENSP00000506839.1:p.Thr76Ile
ENST00000445105.7:c.299C>T MANE Select	ENSP00000393686.1:p.Thr100Ile
ENST00000418610.1:c.299C>T	ENSP00000395517.1:p.Thr100Ile
ENST00000430714.5:c.188C>T	ENSP00000410125.1:p.Thr63Ile
ENST00000440901.4:n.170C>T
ENST00000445105.6:c.299C>T	ENSP00000393686.1:p.Thr100Ile
ENST00000448795.5:c.227C>T	ENSP00000412904.1:p.Thr76Ile
ENST00000450716.5:c.299C>T	ENSP00000397635.1:p.Thr100Ile
ENST00000454309.6:c.485C>T	ENSP00000413496.2:p.Thr162Ile
NM_004113.5:c.299C>T	NP_004104.3:p.Thr100Ile
NM_021032.4:c.485C>T	NP_066360.1:p.Thr162Ile
XM_005247227.1:c.377C>T	XP_005247284.1:p.Thr126Ile
XM_006713538.2:c.290C>T	XP_006713601.1:p.Thr97Ile
XM_006713539.2:c.227C>T	XP_006713602.1:p.Thr76Ile
XM_005247227.2:c.377C>T	XP_005247284.1:p.Thr126Ile
XM_006713538.3:c.290C>T	XP_006713601.1:p.Thr97Ile
XM_024453395.1:c.227C>T	XP_024309163.1:p.Thr76Ile
NM_001377292.1:c.188C>T	NP_001364221.1:p.Thr63Ile
NM_001377293.1:c.227C>T	NP_001364222.1:p.Thr76Ile
NM_001377294.1:c.227C>T	NP_001364223.1:p.Thr76Ile
NM_004113.6:c.299C>T MANE Select	NP_004104.3:p.Thr100Ile
NM_021032.5:c.485C>T	NP_066360.1:p.Thr162Ile