Canonical Allele Identifier: CA355866065

Gene: FGF12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192170560G>A , CM000665.2:g.192170560G>A	GRCh38
NC_000003.11:g.191888349G>A , CM000665.1:g.191888349G>A	GRCh37
NC_000003.10:g.193371043G>A	NCBI36
NG_051966.1:g.562040C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454309.7:c.511C>T	ENSP00000413496.2:p.Arg171Ter
ENST00000683451.2:c.325C>T	ENSP00000508366.1:p.Arg109Ter
ENST00000682572.1:n.417-26433C>T
ENST00000683451.1:c.325C>T	ENSP00000508366.1:p.Arg109Ter
ENST00000683935.1:c.325C>T	ENSP00000507098.1:p.Arg109Ter
ENST00000684282.1:c.253C>T	ENSP00000507149.1:p.Arg85Ter
ENST00000684728.1:c.253C>T	ENSP00000506839.1:p.Arg85Ter
ENST00000445105.7:c.325C>T MANE Select	ENSP00000393686.1:p.Arg109Ter
ENST00000430714.5:c.214C>T	ENSP00000410125.1:p.Arg72Ter
ENST00000440901.4:n.196C>T
ENST00000445105.6:c.325C>T	ENSP00000393686.1:p.Arg109Ter
ENST00000448795.5:c.253C>T	ENSP00000412904.1:p.Arg85Ter
ENST00000450716.5:c.325C>T	ENSP00000397635.1:p.Arg109Ter
ENST00000454309.6:c.511C>T	ENSP00000413496.2:p.Arg171Ter
NM_004113.5:c.325C>T	NP_004104.3:p.Arg109Ter
NM_021032.4:c.511C>T	NP_066360.1:p.Arg171Ter
XM_005247227.1:c.403C>T	XP_005247284.1:p.Arg135Ter
XM_006713538.2:c.316C>T	XP_006713601.1:p.Arg106Ter
XM_006713539.2:c.253C>T	XP_006713602.1:p.Arg85Ter
XM_005247227.2:c.403C>T	XP_005247284.1:p.Arg135Ter
XM_006713538.3:c.316C>T	XP_006713601.1:p.Arg106Ter
XM_024453395.1:c.253C>T	XP_024309163.1:p.Arg85Ter
NM_001377292.1:c.214C>T	NP_001364221.1:p.Arg72Ter
NM_001377293.1:c.253C>T	NP_001364222.1:p.Arg85Ter
NM_001377294.1:c.253C>T	NP_001364223.1:p.Arg85Ter
NM_004113.6:c.325C>T MANE Select	NP_004104.3:p.Arg109Ter
NM_021032.5:c.511C>T	NP_066360.1:p.Arg171Ter