Canonical Allele Identifier: CA1220026676

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128403C= , CM000663.2:g.202128403C=	GRCh38
NC_000001.10:g.202097531C= , CM000663.1:g.202097531C=	GRCh37
NC_000001.9:g.200364154C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.874C=
ENST00000682545.1:c.*299C=	ENSP00000508402.1:n.*299C=
ENST00000682887.1:c.1694C=	ENSP00000506946.1:n.1694C=
ENST00000683302.1:c.1224C=	ENSP00000507885.1:p.Cys408=
ENST00000683557.1:c.*125C=	ENSP00000508029.1:n.*125C=
ENST00000367282.6:c.1293C= MANE Select	ENSP00000356251.4:p.Cys431=
ENST00000367282.5:c.1293C=	ENSP00000356251.4:p.Cys431=
NM_004767.3:c.1293C=	NP_004758.3:p.Cys431=
XM_011510158.1:c.732C=	XP_011508460.1:p.Cys244=
NM_004767.4:c.1293C=	NP_004758.3:p.Cys431=
XM_011510158.2:c.732C=	XP_011508460.1:p.Cys244=
NM_004767.5:c.1293C= MANE Select	NP_004758.3:p.Cys431=