Canonical Allele Identifier: CA344236198

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1395673793
• gnomAD v2: 1-202097574-T-A
• gnomAD v4: 1-202128446-T-A
• MyVariant Identifiers: chr1:g.202097574T>A (hg19) ; chr1:g.202128446T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128446T>A , CM000663.2:g.202128446T>A	GRCh38
NC_000001.10:g.202097574T>A , CM000663.1:g.202097574T>A	GRCh37
NC_000001.9:g.200364197T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.917T>A
ENST00000682545.1:c.*342T>A	ENSP00000508402.1:n.*342T>A
ENST00000682887.1:c.1737T>A	ENSP00000506946.1:n.1737T>A
ENST00000683302.1:c.1267T>A	ENSP00000507885.1:p.Ser423Thr
ENST00000683557.1:c.*168T>A	ENSP00000508029.1:n.*168T>A
ENST00000367282.6:c.1336T>A MANE Select	ENSP00000356251.4:p.Ser446Thr
ENST00000367282.5:c.1336T>A	ENSP00000356251.4:p.Ser446Thr
NM_004767.3:c.1336T>A	NP_004758.3:p.Ser446Thr
XM_011510158.1:c.775T>A	XP_011508460.1:p.Ser259Thr
NM_004767.4:c.1336T>A	NP_004758.3:p.Ser446Thr
XM_011510158.2:c.775T>A	XP_011508460.1:p.Ser259Thr
NM_004767.5:c.1336T>A MANE Select	NP_004758.3:p.Ser446Thr