Canonical Allele Identifier: CA2091241794

Gene: FAM124A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51250100T= , CM000675.2:g.51250100T=	GRCh38
NC_000013.10:g.51824236T= , CM000675.1:g.51824236T=	GRCh37
NC_000013.9:g.50722237T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000322475.13:c.101-1368T= MANE Select	ENSP00000324625.8:n.101-1368T=
ENST00000280057.6:c.209-1368T=	ENSP00000280057.6:n.209-1368T=
ENST00000322475.12:c.101-1368T=	ENSP00000324625.7:n.101-1368T=
ENST00000614765.4:c.101-1368T=	ENSP00000483855.1:n.101-1368T=
ENST00000615498.4:c.101-1368T=	ENSP00000481212.1:n.101-1368T=
NM_001242312.1:c.101-1368T=	NP_001229241.1:n.101-1368T=
NM_145019.3:c.209-1368T=	NP_659456.3:n.209-1368T=
XM_011534974.1:c.89-1368T=	XP_011533276.1:n.89-1368T=
XM_011534975.1:c.89-1368T=	XP_011533277.1:n.89-1368T=
XM_011534976.1:c.89-1368T=	XP_011533278.1:n.89-1368T=
XM_011534977.1:c.89-1368T=	XP_011533279.1:n.89-1368T=
XM_011534978.1:c.209-1368T=	XP_011533280.1:n.209-1368T=
XM_011534979.1:c.209-1368T=	XP_011533281.1:n.209-1368T=
XM_011534980.1:c.209-1368T=	XP_011533282.1:n.209-1368T=
NM_001330522.1:c.101-1368T=	NP_001317451.1:n.101-1368T=
XM_011534978.2:c.209-1368T=	XP_011533280.1:n.209-1368T=
XM_017020419.2:c.101-1368T=	XP_016875908.1:n.101-1368T=
NM_001242312.2:c.101-1368T= MANE Select	NP_001229241.1:n.101-1368T=
NM_145019.4:c.209-1368T=	NP_659456.3:n.209-1368T=
NM_001330522.2:c.101-1368T=	NP_001317451.1:n.101-1368T=