Canonical Allele Identifier: CA1148479132

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128411G= , CM000663.2:g.202128411G=	GRCh38
NC_000001.10:g.202097539G= , CM000663.1:g.202097539G=	GRCh37
NC_000001.9:g.200364162G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.882G=
ENST00000682545.1:c.*307G=	ENSP00000508402.1:n.*307G=
ENST00000682887.1:c.1702G=	ENSP00000506946.1:n.1702G=
ENST00000683302.1:c.1232G=	ENSP00000507885.1:p.Cys411=
ENST00000683557.1:c.*133G=	ENSP00000508029.1:n.*133G=
ENST00000367282.6:c.1301G= MANE Select	ENSP00000356251.4:p.Cys434=
ENST00000367282.5:c.1301G=	ENSP00000356251.4:p.Cys434=
NM_004767.3:c.1301G=	NP_004758.3:p.Cys434=
XM_011510158.1:c.740G=	XP_011508460.1:p.Cys247=
NM_004767.4:c.1301G=	NP_004758.3:p.Cys434=
XM_011510158.2:c.740G=	XP_011508460.1:p.Cys247=
NM_004767.5:c.1301G= MANE Select	NP_004758.3:p.Cys434=