Canonical Allele Identifier: CA1220026678

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128418T= , CM000663.2:g.202128418T=	GRCh38
NC_000001.10:g.202097546T= , CM000663.1:g.202097546T=	GRCh37
NC_000001.9:g.200364169T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.889T=
ENST00000682545.1:c.*314T=	ENSP00000508402.1:n.*314T=
ENST00000682887.1:c.1709T=	ENSP00000506946.1:n.1709T=
ENST00000683302.1:c.1239T=	ENSP00000507885.1:p.Cys413=
ENST00000683557.1:c.*140T=	ENSP00000508029.1:n.*140T=
ENST00000367282.6:c.1308T= MANE Select	ENSP00000356251.4:p.Cys436=
ENST00000367282.5:c.1308T=	ENSP00000356251.4:p.Cys436=
NM_004767.3:c.1308T=	NP_004758.3:p.Cys436=
XM_011510158.1:c.747T=	XP_011508460.1:p.Cys249=
NM_004767.4:c.1308T=	NP_004758.3:p.Cys436=
XM_011510158.2:c.747T=	XP_011508460.1:p.Cys249=
NM_004767.5:c.1308T= MANE Select	NP_004758.3:p.Cys436=