Canonical Allele Identifier: CA1330225

Gene: GPR37L1

Linked Data

• dbSNP Id: rs200746512
• ExAC: 1:202097558 C / A
• gnomAD v2: 1-202097558-C-A
• gnomAD v3: 1-202128430-C-A
• gnomAD v4: 1-202128430-C-A
• MyVariant Identifiers: chr1:g.202097558C>A (hg19) ; chr1:g.202128430C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128430C>A , CM000663.2:g.202128430C>A	GRCh38
NC_000001.10:g.202097558C>A , CM000663.1:g.202097558C>A	GRCh37
NC_000001.9:g.200364181C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.901C>A
ENST00000682545.1:c.*326C>A	ENSP00000508402.1:n.*326C>A
ENST00000682887.1:c.1721C>A	ENSP00000506946.1:n.1721C>A
ENST00000683302.1:c.1251C>A	ENSP00000507885.1:p.Gly417=
ENST00000683557.1:c.*152C>A	ENSP00000508029.1:n.*152C>A
ENST00000367282.6:c.1320C>A MANE Select	ENSP00000356251.4:p.Gly440=
ENST00000367282.5:c.1320C>A	ENSP00000356251.4:p.Gly440=
NM_004767.3:c.1320C>A	NP_004758.3:p.Gly440=
XM_011510158.1:c.759C>A	XP_011508460.1:p.Gly253=
NM_004767.4:c.1320C>A	NP_004758.3:p.Gly440=
XM_011510158.2:c.759C>A	XP_011508460.1:p.Gly253=
NM_004767.5:c.1320C>A MANE Select	NP_004758.3:p.Gly440=