Canonical Allele Identifier: CA1220026682

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128425T= , CM000663.2:g.202128425T=	GRCh38
NC_000001.10:g.202097553T= , CM000663.1:g.202097553T=	GRCh37
NC_000001.9:g.200364176T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.896T=
ENST00000682545.1:c.*321T=	ENSP00000508402.1:n.*321T=
ENST00000682887.1:c.1716T=	ENSP00000506946.1:n.1716T=
ENST00000683302.1:c.1246T=	ENSP00000507885.1:p.Cys416=
ENST00000683557.1:c.*147T=	ENSP00000508029.1:n.*147T=
ENST00000367282.6:c.1315T= MANE Select	ENSP00000356251.4:p.Cys439=
ENST00000367282.5:c.1315T=	ENSP00000356251.4:p.Cys439=
NM_004767.3:c.1315T=	NP_004758.3:p.Cys439=
XM_011510158.1:c.754T=	XP_011508460.1:p.Cys252=
NM_004767.4:c.1315T=	NP_004758.3:p.Cys439=
XM_011510158.2:c.754T=	XP_011508460.1:p.Cys252=
NM_004767.5:c.1315T= MANE Select	NP_004758.3:p.Cys439=