Canonical Allele Identifier: CA1330226

Gene: GPR37L1

Linked Data

• dbSNP Id: rs61734417
• ExAC: 1:202097559 G / A
• gnomAD v2: 1-202097559-G-A
• gnomAD v3: 1-202128431-G-A
• gnomAD v4: 1-202128431-G-A
• MyVariant Identifiers: chr1:g.202097559G>A (hg19) ; chr1:g.202128431G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.902G>A
ENST00000682545.1:c.*327G>A	ENSP00000508402.1:n.*327G>A
ENST00000682887.1:c.1722G>A	ENSP00000506946.1:n.1722G>A
ENST00000683302.1:c.1252G>A	ENSP00000507885.1:p.Gly418Arg
ENST00000683557.1:c.*153G>A	ENSP00000508029.1:n.*153G>A
ENST00000367282.6:c.1321G>A MANE Select	ENSP00000356251.4:p.Gly441Arg
ENST00000367282.5:c.1321G>A	ENSP00000356251.4:p.Gly441Arg
NM_004767.3:c.1321G>A	NP_004758.3:p.Gly441Arg
XM_011510158.1:c.760G>A	XP_011508460.1:p.Gly254Arg
NM_004767.4:c.1321G>A	NP_004758.3:p.Gly441Arg
XM_011510158.2:c.760G>A	XP_011508460.1:p.Gly254Arg
NM_004767.5:c.1321G>A MANE Select	NP_004758.3:p.Gly441Arg