Canonical Allele Identifier: CA1330221

Gene: GPR37L1

Linked Data

• dbSNP Id: rs767258187
• ExAC: 1:202097552 G / A
• gnomAD v2: 1-202097552-G-A
• gnomAD v3: 1-202128424-G-A
• gnomAD v4: 1-202128424-G-A
• MyVariant Identifiers: chr1:g.202097552G>A (hg19) ; chr1:g.202128424G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128424G>A , CM000663.2:g.202128424G>A	GRCh38
NC_000001.10:g.202097552G>A , CM000663.1:g.202097552G>A	GRCh37
NC_000001.9:g.200364175G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.895G>A
ENST00000682545.1:c.*320G>A	ENSP00000508402.1:n.*320G>A
ENST00000682887.1:c.1715G>A	ENSP00000506946.1:n.1715G>A
ENST00000683302.1:c.1245G>A	ENSP00000507885.1:p.Glu415=
ENST00000683557.1:c.*146G>A	ENSP00000508029.1:n.*146G>A
ENST00000367282.6:c.1314G>A MANE Select	ENSP00000356251.4:p.Glu438=
ENST00000367282.5:c.1314G>A	ENSP00000356251.4:p.Glu438=
NM_004767.3:c.1314G>A	NP_004758.3:p.Glu438=
XM_011510158.1:c.753G>A	XP_011508460.1:p.Glu251=
NM_004767.4:c.1314G>A	NP_004758.3:p.Glu438=
XM_011510158.2:c.753G>A	XP_011508460.1:p.Glu251=
NM_004767.5:c.1314G>A MANE Select	NP_004758.3:p.Glu438=