Canonical Allele Identifier: CA1330191

Gene: GPR37L1

Linked Data

• dbSNP Id: rs377493703
• ExAC: 1:202097407 C / G
• gnomAD v2: 1-202097407-C-G
• gnomAD v4: 1-202128279-C-G
• MyVariant Identifiers: chr1:g.202097407C>G (hg19) ; chr1:g.202128279C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128279C>G , CM000663.2:g.202128279C>G	GRCh38
NC_000001.10:g.202097407C>G , CM000663.1:g.202097407C>G	GRCh37
NC_000001.9:g.200364030C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.750C>G
ENST00000682545.1:c.*175C>G	ENSP00000508402.1:n.*175C>G
ENST00000682887.1:c.1570C>G	ENSP00000506946.1:n.1570C>G
ENST00000683302.1:c.1100C>G	ENSP00000507885.1:p.Thr367Ser
ENST00000683557.1:c.*1C>G	ENSP00000508029.1:n.*1C>G
ENST00000367282.6:c.1169C>G MANE Select	ENSP00000356251.4:p.Thr390Ser
ENST00000367282.5:c.1169C>G	ENSP00000356251.4:p.Thr390Ser
NM_004767.3:c.1169C>G	NP_004758.3:p.Thr390Ser
XM_011510158.1:c.608C>G	XP_011508460.1:p.Thr203Ser
NM_004767.4:c.1169C>G	NP_004758.3:p.Thr390Ser
XM_011510158.2:c.608C>G	XP_011508460.1:p.Thr203Ser
NM_004767.5:c.1169C>G MANE Select	NP_004758.3:p.Thr390Ser