Canonical Allele Identifier: CA1220026685

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128428G= , CM000663.2:g.202128428G=	GRCh38
NC_000001.10:g.202097556G= , CM000663.1:g.202097556G=	GRCh37
NC_000001.9:g.200364179G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.899G=
ENST00000682545.1:c.*324G=	ENSP00000508402.1:n.*324G=
ENST00000682887.1:c.1719G=	ENSP00000506946.1:n.1719G=
ENST00000683302.1:c.1249G=	ENSP00000507885.1:p.Gly417=
ENST00000683557.1:c.*150G=	ENSP00000508029.1:n.*150G=
ENST00000367282.6:c.1318G= MANE Select	ENSP00000356251.4:p.Gly440=
ENST00000367282.5:c.1318G=	ENSP00000356251.4:p.Gly440=
NM_004767.3:c.1318G=	NP_004758.3:p.Gly440=
XM_011510158.1:c.757G=	XP_011508460.1:p.Gly253=
NM_004767.4:c.1318G=	NP_004758.3:p.Gly440=
XM_011510158.2:c.757G=	XP_011508460.1:p.Gly253=
NM_004767.5:c.1318G= MANE Select	NP_004758.3:p.Gly440=