Canonical Allele Identifier: CA1330197

Gene: GPR37L1

Linked Data

• dbSNP Id: rs762811498
• ExAC: 1:202097452 C / A
• gnomAD v2: 1-202097452-C-A
• gnomAD v3: 1-202128324-C-A
• gnomAD v4: 1-202128324-C-A
• MyVariant Identifiers: chr1:g.202097452C>A (hg19) ; chr1:g.202128324C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128324C>A , CM000663.2:g.202128324C>A	GRCh38
NC_000001.10:g.202097452C>A , CM000663.1:g.202097452C>A	GRCh37
NC_000001.9:g.200364075C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.795C>A
ENST00000682545.1:c.*220C>A	ENSP00000508402.1:n.*220C>A
ENST00000682887.1:c.1615C>A	ENSP00000506946.1:n.1615C>A
ENST00000683302.1:c.1145C>A	ENSP00000507885.1:p.Thr382Asn
ENST00000683557.1:c.*46C>A	ENSP00000508029.1:n.*46C>A
ENST00000367282.6:c.1214C>A MANE Select	ENSP00000356251.4:p.Thr405Asn
ENST00000367282.5:c.1214C>A	ENSP00000356251.4:p.Thr405Asn
NM_004767.3:c.1214C>A	NP_004758.3:p.Thr405Asn
XM_011510158.1:c.653C>A	XP_011508460.1:p.Thr218Asn
NM_004767.4:c.1214C>A	NP_004758.3:p.Thr405Asn
XM_011510158.2:c.653C>A	XP_011508460.1:p.Thr218Asn
NM_004767.5:c.1214C>A MANE Select	NP_004758.3:p.Thr405Asn