Canonical Allele Identifier: CA1220026648

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128302G= , CM000663.2:g.202128302G=	GRCh38
NC_000001.10:g.202097430G= , CM000663.1:g.202097430G=	GRCh37
NC_000001.9:g.200364053G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.773G=
ENST00000682545.1:c.*198G=	ENSP00000508402.1:n.*198G=
ENST00000682887.1:c.1593G=	ENSP00000506946.1:n.1593G=
ENST00000683302.1:c.1123G=	ENSP00000507885.1:p.Gly375=
ENST00000683557.1:c.*24G=	ENSP00000508029.1:n.*24G=
ENST00000367282.6:c.1192G= MANE Select	ENSP00000356251.4:p.Gly398=
ENST00000367282.5:c.1192G=	ENSP00000356251.4:p.Gly398=
NM_004767.3:c.1192G=	NP_004758.3:p.Gly398=
XM_011510158.1:c.631G=	XP_011508460.1:p.Gly211=
NM_004767.4:c.1192G=	NP_004758.3:p.Gly398=
XM_011510158.2:c.631G=	XP_011508460.1:p.Gly211=
NM_004767.5:c.1192G= MANE Select	NP_004758.3:p.Gly398=