Canonical Allele Identifier: CA1140725297

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128431G= , CM000663.2:g.202128431G=	GRCh38
NC_000001.10:g.202097559G= , CM000663.1:g.202097559G=	GRCh37
NC_000001.9:g.200364182G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.902G=
ENST00000682545.1:c.*327G=	ENSP00000508402.1:n.*327G=
ENST00000682887.1:c.1722G=	ENSP00000506946.1:n.1722G=
ENST00000683302.1:c.1252G=	ENSP00000507885.1:p.Gly418=
ENST00000683557.1:c.*153G=	ENSP00000508029.1:n.*153G=
ENST00000367282.6:c.1321G= MANE Select	ENSP00000356251.4:p.Gly441=
ENST00000367282.5:c.1321G=	ENSP00000356251.4:p.Gly441=
NM_004767.3:c.1321G=	NP_004758.3:p.Gly441=
XM_011510158.1:c.760G=	XP_011508460.1:p.Gly254=
NM_004767.4:c.1321G=	NP_004758.3:p.Gly441=
XM_011510158.2:c.760G=	XP_011508460.1:p.Gly254=
NM_004767.5:c.1321G= MANE Select	NP_004758.3:p.Gly441=