Canonical Allele Identifier: CA344236158

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1272741485
• gnomAD v3: 1-202128426-G-A
• gnomAD v4: 1-202128426-G-A
• MyVariant Identifiers: chr1:g.202097554G>A (hg19) ; chr1:g.202128426G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128426G>A , CM000663.2:g.202128426G>A	GRCh38
NC_000001.10:g.202097554G>A , CM000663.1:g.202097554G>A	GRCh37
NC_000001.9:g.200364177G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.897G>A
ENST00000682545.1:c.*322G>A	ENSP00000508402.1:n.*322G>A
ENST00000682887.1:c.1717G>A	ENSP00000506946.1:n.1717G>A
ENST00000683302.1:c.1247G>A	ENSP00000507885.1:p.Cys416Tyr
ENST00000683557.1:c.*148G>A	ENSP00000508029.1:n.*148G>A
ENST00000367282.6:c.1316G>A MANE Select	ENSP00000356251.4:p.Cys439Tyr
ENST00000367282.5:c.1316G>A	ENSP00000356251.4:p.Cys439Tyr
NM_004767.3:c.1316G>A	NP_004758.3:p.Cys439Tyr
XM_011510158.1:c.755G>A	XP_011508460.1:p.Cys252Tyr
NM_004767.4:c.1316G>A	NP_004758.3:p.Cys439Tyr
XM_011510158.2:c.755G>A	XP_011508460.1:p.Cys252Tyr
NM_004767.5:c.1316G>A MANE Select	NP_004758.3:p.Cys439Tyr