Canonical Allele Identifier: CA1220026695

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128451T= , CM000663.2:g.202128451T=	GRCh38
NC_000001.10:g.202097579T= , CM000663.1:g.202097579T=	GRCh37
NC_000001.9:g.200364202T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.922T=
ENST00000682545.1:c.*347T=	ENSP00000508402.1:n.*347T=
ENST00000682887.1:c.1742T=	ENSP00000506946.1:n.1742T=
ENST00000683302.1:c.1272T=	ENSP00000507885.1:p.Ala424=
ENST00000683557.1:c.*173T=	ENSP00000508029.1:n.*173T=
ENST00000367282.6:c.1341T= MANE Select	ENSP00000356251.4:p.Ala447=
ENST00000367282.5:c.1341T=	ENSP00000356251.4:p.Ala447=
NM_004767.3:c.1341T=	NP_004758.3:p.Ala447=
XM_011510158.1:c.780T=	XP_011508460.1:p.Ala260=
NM_004767.4:c.1341T=	NP_004758.3:p.Ala447=
XM_011510158.2:c.780T=	XP_011508460.1:p.Ala260=
NM_004767.5:c.1341T= MANE Select	NP_004758.3:p.Ala447=