Canonical Allele Identifier: CA1220026649

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128305C= , CM000663.2:g.202128305C=	GRCh38
NC_000001.10:g.202097433C= , CM000663.1:g.202097433C=	GRCh37
NC_000001.9:g.200364056C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.776C=
ENST00000682545.1:c.*201C=	ENSP00000508402.1:n.*201C=
ENST00000682887.1:c.1596C=	ENSP00000506946.1:n.1596C=
ENST00000683302.1:c.1126C=	ENSP00000507885.1:p.Leu376=
ENST00000683557.1:c.*27C=	ENSP00000508029.1:n.*27C=
ENST00000367282.6:c.1195C= MANE Select	ENSP00000356251.4:p.Leu399=
ENST00000367282.5:c.1195C=	ENSP00000356251.4:p.Leu399=
NM_004767.3:c.1195C=	NP_004758.3:p.Leu399=
XM_011510158.1:c.634C=	XP_011508460.1:p.Leu212=
NM_004767.4:c.1195C=	NP_004758.3:p.Leu399=
XM_011510158.2:c.634C=	XP_011508460.1:p.Leu212=
NM_004767.5:c.1195C= MANE Select	NP_004758.3:p.Leu399=