Canonical Allele Identifier: CA1220026672

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128392C= , CM000663.2:g.202128392C=	GRCh38
NC_000001.10:g.202097520C= , CM000663.1:g.202097520C=	GRCh37
NC_000001.9:g.200364143C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.863C=
ENST00000682545.1:c.*288C=	ENSP00000508402.1:n.*288C=
ENST00000682887.1:c.1683C=	ENSP00000506946.1:n.1683C=
ENST00000683302.1:c.1213C=	ENSP00000507885.1:p.Leu405=
ENST00000683557.1:c.*114C=	ENSP00000508029.1:n.*114C=
ENST00000367282.6:c.1282C= MANE Select	ENSP00000356251.4:p.Leu428=
ENST00000367282.5:c.1282C=	ENSP00000356251.4:p.Leu428=
NM_004767.3:c.1282C=	NP_004758.3:p.Leu428=
XM_011510158.1:c.721C=	XP_011508460.1:p.Leu241=
NM_004767.4:c.1282C=	NP_004758.3:p.Leu428=
XM_011510158.2:c.721C=	XP_011508460.1:p.Leu241=
NM_004767.5:c.1282C= MANE Select	NP_004758.3:p.Leu428=