Canonical Allele Identifier: CA1220026651

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128311A= , CM000663.2:g.202128311A=	GRCh38
NC_000001.10:g.202097439A= , CM000663.1:g.202097439A=	GRCh37
NC_000001.9:g.200364062A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.782A=
ENST00000682545.1:c.*207A=	ENSP00000508402.1:n.*207A=
ENST00000682887.1:c.1602A=	ENSP00000506946.1:n.1602A=
ENST00000683302.1:c.1132A=	ENSP00000507885.1:p.Asn378=
ENST00000683557.1:c.*33A=	ENSP00000508029.1:n.*33A=
ENST00000367282.6:c.1201A= MANE Select	ENSP00000356251.4:p.Asn401=
ENST00000367282.5:c.1201A=	ENSP00000356251.4:p.Asn401=
NM_004767.3:c.1201A=	NP_004758.3:p.Asn401=
XM_011510158.1:c.640A=	XP_011508460.1:p.Asn214=
NM_004767.4:c.1201A=	NP_004758.3:p.Asn401=
XM_011510158.2:c.640A=	XP_011508460.1:p.Asn214=
NM_004767.5:c.1201A= MANE Select	NP_004758.3:p.Asn401=