Canonical Allele Identifier: CA1220026626

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128219T= , CM000663.2:g.202128219T=	GRCh38
NC_000001.10:g.202097347T= , CM000663.1:g.202097347T=	GRCh37
NC_000001.9:g.200363970T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.705-15T=
ENST00000682545.1:c.*115T=	ENSP00000508402.1:n.*115T=
ENST00000682887.1:c.1510T=	ENSP00000506946.1:n.1510T=
ENST00000683302.1:c.1040T=	ENSP00000507885.1:p.Phe347=
ENST00000683557.1:c.715-15T=	ENSP00000508029.1:n.715-15T=
ENST00000367282.6:c.1109T= MANE Select	ENSP00000356251.4:p.Phe370=
ENST00000367282.5:c.1109T=	ENSP00000356251.4:p.Phe370=
NM_004767.3:c.1109T=	NP_004758.3:p.Phe370=
XM_011510158.1:c.548T=	XP_011508460.1:p.Phe183=
NM_004767.4:c.1109T=	NP_004758.3:p.Phe370=
XM_011510158.2:c.548T=	XP_011508460.1:p.Phe183=
NM_004767.5:c.1109T= MANE Select	NP_004758.3:p.Phe370=