Canonical Allele Identifier: CA1220026669

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128378T= , CM000663.2:g.202128378T=	GRCh38
NC_000001.10:g.202097506T= , CM000663.1:g.202097506T=	GRCh37
NC_000001.9:g.200364129T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.849T=
ENST00000682545.1:c.*274T=	ENSP00000508402.1:n.*274T=
ENST00000682887.1:c.1669T=	ENSP00000506946.1:n.1669T=
ENST00000683302.1:c.1199T=	ENSP00000507885.1:p.Leu400=
ENST00000683557.1:c.*100T=	ENSP00000508029.1:n.*100T=
ENST00000367282.6:c.1268T= MANE Select	ENSP00000356251.4:p.Leu423=
ENST00000367282.5:c.1268T=	ENSP00000356251.4:p.Leu423=
NM_004767.3:c.1268T=	NP_004758.3:p.Leu423=
XM_011510158.1:c.707T=	XP_011508460.1:p.Leu236=
NM_004767.4:c.1268T=	NP_004758.3:p.Leu423=
XM_011510158.2:c.707T=	XP_011508460.1:p.Leu236=
NM_004767.5:c.1268T= MANE Select	NP_004758.3:p.Leu423=