Canonical Allele Identifier: CA344235928

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1216647834
• gnomAD v3: 1-202128323-A-T
• gnomAD v4: 1-202128323-A-T
• MyVariant Identifiers: chr1:g.202097451A>T (hg19) ; chr1:g.202128323A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128323A>T , CM000663.2:g.202128323A>T	GRCh38
NC_000001.10:g.202097451A>T , CM000663.1:g.202097451A>T	GRCh37
NC_000001.9:g.200364074A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.794A>T
ENST00000682545.1:c.*219A>T	ENSP00000508402.1:n.*219A>T
ENST00000682887.1:c.1614A>T	ENSP00000506946.1:n.1614A>T
ENST00000683302.1:c.1144A>T	ENSP00000507885.1:p.Thr382Ser
ENST00000683557.1:c.*45A>T	ENSP00000508029.1:n.*45A>T
ENST00000367282.6:c.1213A>T MANE Select	ENSP00000356251.4:p.Thr405Ser
ENST00000367282.5:c.1213A>T	ENSP00000356251.4:p.Thr405Ser
NM_004767.3:c.1213A>T	NP_004758.3:p.Thr405Ser
XM_011510158.1:c.652A>T	XP_011508460.1:p.Thr218Ser
NM_004767.4:c.1213A>T	NP_004758.3:p.Thr405Ser
XM_011510158.2:c.652A>T	XP_011508460.1:p.Thr218Ser
NM_004767.5:c.1213A>T MANE Select	NP_004758.3:p.Thr405Ser