Canonical Allele Identifier: CA1220026680

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128423A= , CM000663.2:g.202128423A=	GRCh38
NC_000001.10:g.202097551A= , CM000663.1:g.202097551A=	GRCh37
NC_000001.9:g.200364174A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.894A=
ENST00000682545.1:c.*319A=	ENSP00000508402.1:n.*319A=
ENST00000682887.1:c.1714A=	ENSP00000506946.1:n.1714A=
ENST00000683302.1:c.1244A=	ENSP00000507885.1:p.Glu415=
ENST00000683557.1:c.*145A=	ENSP00000508029.1:n.*145A=
ENST00000367282.6:c.1313A= MANE Select	ENSP00000356251.4:p.Glu438=
ENST00000367282.5:c.1313A=	ENSP00000356251.4:p.Glu438=
NM_004767.3:c.1313A=	NP_004758.3:p.Glu438=
XM_011510158.1:c.752A=	XP_011508460.1:p.Glu251=
NM_004767.4:c.1313A=	NP_004758.3:p.Glu438=
XM_011510158.2:c.752A=	XP_011508460.1:p.Glu251=
NM_004767.5:c.1313A= MANE Select	NP_004758.3:p.Glu438=