Canonical Allele Identifier: CA1220026639

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128281C= , CM000663.2:g.202128281C=	GRCh38
NC_000001.10:g.202097409C= , CM000663.1:g.202097409C=	GRCh37
NC_000001.9:g.200364032C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.752C=
ENST00000682545.1:c.*177C=	ENSP00000508402.1:n.*177C=
ENST00000682887.1:c.1572C=	ENSP00000506946.1:n.1572C=
ENST00000683302.1:c.1102C=	ENSP00000507885.1:p.Arg368=
ENST00000683557.1:c.*3C=	ENSP00000508029.1:n.*3C=
ENST00000367282.6:c.1171C= MANE Select	ENSP00000356251.4:p.Arg391=
ENST00000367282.5:c.1171C=	ENSP00000356251.4:p.Arg391=
NM_004767.3:c.1171C=	NP_004758.3:p.Arg391=
XM_011510158.1:c.610C=	XP_011508460.1:p.Arg204=
NM_004767.4:c.1171C=	NP_004758.3:p.Arg391=
XM_011510158.2:c.610C=	XP_011508460.1:p.Arg204=
NM_004767.5:c.1171C= MANE Select	NP_004758.3:p.Arg391=