Canonical Allele Identifier: CA1220026677

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128414G= , CM000663.2:g.202128414G=	GRCh38
NC_000001.10:g.202097542G= , CM000663.1:g.202097542G=	GRCh37
NC_000001.9:g.200364165G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.885G=
ENST00000682545.1:c.*310G=	ENSP00000508402.1:n.*310G=
ENST00000682887.1:c.1705G=	ENSP00000506946.1:n.1705G=
ENST00000683302.1:c.1235G=	ENSP00000507885.1:p.Cys412=
ENST00000683557.1:c.*136G=	ENSP00000508029.1:n.*136G=
ENST00000367282.6:c.1304G= MANE Select	ENSP00000356251.4:p.Cys435=
ENST00000367282.5:c.1304G=	ENSP00000356251.4:p.Cys435=
NM_004767.3:c.1304G=	NP_004758.3:p.Cys435=
XM_011510158.1:c.743G=	XP_011508460.1:p.Cys248=
NM_004767.4:c.1304G=	NP_004758.3:p.Cys435=
XM_011510158.2:c.743G=	XP_011508460.1:p.Cys248=
NM_004767.5:c.1304G= MANE Select	NP_004758.3:p.Cys435=