Canonical Allele Identifier: CA1220026644

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128293G= , CM000663.2:g.202128293G=	GRCh38
NC_000001.10:g.202097421G= , CM000663.1:g.202097421G=	GRCh37
NC_000001.9:g.200364044G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.764G=
ENST00000682545.1:c.*189G=	ENSP00000508402.1:n.*189G=
ENST00000682887.1:c.1584G=	ENSP00000506946.1:n.1584G=
ENST00000683302.1:c.1114G=	ENSP00000507885.1:p.Asp372=
ENST00000683557.1:c.*15G=	ENSP00000508029.1:n.*15G=
ENST00000367282.6:c.1183G= MANE Select	ENSP00000356251.4:p.Asp395=
ENST00000367282.5:c.1183G=	ENSP00000356251.4:p.Asp395=
NM_004767.3:c.1183G=	NP_004758.3:p.Asp395=
XM_011510158.1:c.622G=	XP_011508460.1:p.Asp208=
NM_004767.4:c.1183G=	NP_004758.3:p.Asp395=
XM_011510158.2:c.622G=	XP_011508460.1:p.Asp208=
NM_004767.5:c.1183G= MANE Select	NP_004758.3:p.Asp395=