Canonical Allele Identifier: CA1148449325

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128449G= , CM000663.2:g.202128449G=	GRCh38
NC_000001.10:g.202097577G= , CM000663.1:g.202097577G=	GRCh37
NC_000001.9:g.200364200G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.920G=
ENST00000682545.1:c.*345G=	ENSP00000508402.1:n.*345G=
ENST00000682887.1:c.1740G=	ENSP00000506946.1:n.1740G=
ENST00000683302.1:c.1270G=	ENSP00000507885.1:p.Ala424=
ENST00000683557.1:c.*171G=	ENSP00000508029.1:n.*171G=
ENST00000367282.6:c.1339G= MANE Select	ENSP00000356251.4:p.Ala447=
ENST00000367282.5:c.1339G=	ENSP00000356251.4:p.Ala447=
NM_004767.3:c.1339G=	NP_004758.3:p.Ala447=
XM_011510158.1:c.778G=	XP_011508460.1:p.Ala260=
NM_004767.4:c.1339G=	NP_004758.3:p.Ala447=
XM_011510158.2:c.778G=	XP_011508460.1:p.Ala260=
NM_004767.5:c.1339G= MANE Select	NP_004758.3:p.Ala447=