Canonical Allele Identifier: CA2755795

Gene: FGF12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192335375A>G , CM000665.2:g.192335375A>G	GRCh38
NC_000003.11:g.192053164A>G , CM000665.1:g.192053164A>G	GRCh37
NC_000003.10:g.193535858A>G	NCBI36
NG_051966.1:g.397225T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454309.7:c.400T>C	ENSP00000413496.2:p.Tyr134His
ENST00000682819.2:n.467T>C
ENST00000683451.2:c.214T>C	ENSP00000508366.1:p.Tyr72His
ENST00000682572.1:n.402T>C
ENST00000682819.1:n.433T>C
ENST00000683451.1:c.214T>C	ENSP00000508366.1:p.Tyr72His
ENST00000683935.1:c.214T>C	ENSP00000507098.1:p.Tyr72His
ENST00000684282.1:c.142T>C	ENSP00000507149.1:p.Tyr48His
ENST00000684728.1:c.142T>C	ENSP00000506839.1:p.Tyr48His
ENST00000445105.7:c.214T>C MANE Select	ENSP00000393686.1:p.Tyr72His
ENST00000418610.1:c.214T>C	ENSP00000395517.1:p.Tyr72His
ENST00000430714.5:c.103T>C	ENSP00000410125.1:p.Tyr35His
ENST00000445105.6:c.214T>C	ENSP00000393686.1:p.Tyr72His
ENST00000448795.5:c.142T>C	ENSP00000412904.1:p.Tyr48His
ENST00000450716.5:c.214T>C	ENSP00000397635.1:p.Tyr72His
ENST00000454309.6:c.400T>C	ENSP00000413496.2:p.Tyr134His
NM_004113.5:c.214T>C	NP_004104.3:p.Tyr72His
NM_021032.4:c.400T>C	NP_066360.1:p.Tyr134His
XM_005247227.1:c.292T>C	XP_005247284.1:p.Tyr98His
XM_006713538.2:c.205T>C	XP_006713601.1:p.Tyr69His
XM_006713539.2:c.142T>C	XP_006713602.1:p.Tyr48His
XM_005247227.2:c.292T>C	XP_005247284.1:p.Tyr98His
XM_006713538.3:c.205T>C	XP_006713601.1:p.Tyr69His
XM_024453395.1:c.142T>C	XP_024309163.1:p.Tyr48His
NM_001377292.1:c.103T>C	NP_001364221.1:p.Tyr35His
NM_001377293.1:c.142T>C	NP_001364222.1:p.Tyr48His
NM_001377294.1:c.142T>C	NP_001364223.1:p.Tyr48His
NM_004113.6:c.214T>C MANE Select	NP_004104.3:p.Tyr72His
NM_021032.5:c.400T>C	NP_066360.1:p.Tyr134His