Canonical Allele Identifier: CA1330194

Gene: GPR37L1

Linked Data

• ClinVar Variation Id: 2381882
• ClinVar RCV Id: RCV004221469
• dbSNP Id: rs151200634
• ExAC: 1:202097416 C / T
• gnomAD v2: 1-202097416-C-T
• gnomAD v3: 1-202128288-C-T
• gnomAD v4: 1-202128288-C-T
• MyVariant Identifiers: chr1:g.202097416C>T (hg19) ; chr1:g.202128288C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128288C>T , CM000663.2:g.202128288C>T	GRCh38
NC_000001.10:g.202097416C>T , CM000663.1:g.202097416C>T	GRCh37
NC_000001.9:g.200364039C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.759C>T
ENST00000682545.1:c.*184C>T	ENSP00000508402.1:n.*184C>T
ENST00000682887.1:c.1579C>T	ENSP00000506946.1:n.1579C>T
ENST00000683302.1:c.1109C>T	ENSP00000507885.1:p.Thr370Ile
ENST00000683557.1:c.*10C>T	ENSP00000508029.1:n.*10C>T
ENST00000367282.6:c.1178C>T MANE Select	ENSP00000356251.4:p.Thr393Ile
ENST00000367282.5:c.1178C>T	ENSP00000356251.4:p.Thr393Ile
NM_004767.3:c.1178C>T	NP_004758.3:p.Thr393Ile
XM_011510158.1:c.617C>T	XP_011508460.1:p.Thr206Ile
NM_004767.4:c.1178C>T	NP_004758.3:p.Thr393Ile
XM_011510158.2:c.617C>T	XP_011508460.1:p.Thr206Ile
NM_004767.5:c.1178C>T MANE Select	NP_004758.3:p.Thr393Ile