Canonical Allele Identifier: CA1148895931

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128438C= , CM000663.2:g.202128438C=	GRCh38
NC_000001.10:g.202097566C= , CM000663.1:g.202097566C=	GRCh37
NC_000001.9:g.200364189C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.909C=
ENST00000682545.1:c.*334C=	ENSP00000508402.1:n.*334C=
ENST00000682887.1:c.1729C=	ENSP00000506946.1:n.1729C=
ENST00000683302.1:c.1259C=	ENSP00000507885.1:p.Ser420=
ENST00000683557.1:c.*160C=	ENSP00000508029.1:n.*160C=
ENST00000367282.6:c.1328C= MANE Select	ENSP00000356251.4:p.Ser443=
ENST00000367282.5:c.1328C=	ENSP00000356251.4:p.Ser443=
NM_004767.3:c.1328C=	NP_004758.3:p.Ser443=
XM_011510158.1:c.767C=	XP_011508460.1:p.Ser256=
NM_004767.4:c.1328C=	NP_004758.3:p.Ser443=
XM_011510158.2:c.767C=	XP_011508460.1:p.Ser256=
NM_004767.5:c.1328C= MANE Select	NP_004758.3:p.Ser443=