Canonical Allele Identifier: CA1220026624

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128216C= , CM000663.2:g.202128216C=	GRCh38
NC_000001.10:g.202097344C= , CM000663.1:g.202097344C=	GRCh37
NC_000001.9:g.200363967C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.705-18C=
ENST00000682545.1:c.*112C=	ENSP00000508402.1:n.*112C=
ENST00000682887.1:c.1507C=	ENSP00000506946.1:n.1507C=
ENST00000683302.1:c.1037C=	ENSP00000507885.1:p.Ala346=
ENST00000683557.1:c.715-18C=	ENSP00000508029.1:n.715-18C=
ENST00000367282.6:c.1106C= MANE Select	ENSP00000356251.4:p.Ala369=
ENST00000367282.5:c.1106C=	ENSP00000356251.4:p.Ala369=
NM_004767.3:c.1106C=	NP_004758.3:p.Ala369=
XM_011510158.1:c.545C=	XP_011508460.1:p.Ala182=
NM_004767.4:c.1106C=	NP_004758.3:p.Ala369=
XM_011510158.2:c.545C=	XP_011508460.1:p.Ala182=
NM_004767.5:c.1106C= MANE Select	NP_004758.3:p.Ala369=