Canonical Allele Identifier: CA1330231
Gene: GPR37L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2364175
ClinVar RCV Id: RCV004206353
dbSNP Id: rs747264401
ExAC: 1:202097577 G / A
gnomAD v2: 1-202097577-G-A
gnomAD v3: 1-202128449-G-A
gnomAD v4: 1-202128449-G-A
MyVariant Identifiers: chr1:g.202097577G>A (hg19) chr1:g.202128449G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202128449G>A , CM000663.2:g.202128449G>A GRCh38
NC_000001.10:g.202097577G>A , CM000663.1:g.202097577G>A GRCh37
NC_000001.9:g.200364200G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682422.1:n.920G>A
ENST00000682545.1:c.*345G>A ENSP00000508402.1:n.*345G>A
ENST00000682887.1:c.1740G>A ENSP00000506946.1:n.1740G>A
ENST00000683302.1:c.1270G>A ENSP00000507885.1:p.Ala424Thr
ENST00000683557.1:c.*171G>A ENSP00000508029.1:n.*171G>A
ENST00000367282.6:c.1339G>A MANE Select ENSP00000356251.4:p.Ala447Thr
ENST00000367282.5:c.1339G>A ENSP00000356251.4:p.Ala447Thr
NM_004767.3:c.1339G>A NP_004758.3:p.Ala447Thr
XM_011510158.1:c.778G>A XP_011508460.1:p.Ala260Thr
NM_004767.4:c.1339G>A NP_004758.3:p.Ala447Thr
XM_011510158.2:c.778G>A XP_011508460.1:p.Ala260Thr
NM_004767.5:c.1339G>A MANE Select NP_004758.3:p.Ala447Thr
Search 100 bp 5'
Search 100 bp 3'