Canonical Allele Identifier: CA1330229

Gene: GPR37L1

Linked Data

• dbSNP Id: rs758707358
• ExAC: 1:202097567 G / A
• gnomAD v2: 1-202097567-G-A
• gnomAD v3: 1-202128439-G-A
• gnomAD v4: 1-202128439-G-A
• COSMIC: COSM902291
• MyVariant Identifiers: chr1:g.202097567G>A (hg19) ; chr1:g.202128439G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128439G>A , CM000663.2:g.202128439G>A	GRCh38
NC_000001.10:g.202097567G>A , CM000663.1:g.202097567G>A	GRCh37
NC_000001.9:g.200364190G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.910G>A
ENST00000682545.1:c.*335G>A	ENSP00000508402.1:n.*335G>A
ENST00000682887.1:c.1730G>A	ENSP00000506946.1:n.1730G>A
ENST00000683302.1:c.1260G>A	ENSP00000507885.1:p.Ser420=
ENST00000683557.1:c.*161G>A	ENSP00000508029.1:n.*161G>A
ENST00000367282.6:c.1329G>A MANE Select	ENSP00000356251.4:p.Ser443=
ENST00000367282.5:c.1329G>A	ENSP00000356251.4:p.Ser443=
NM_004767.3:c.1329G>A	NP_004758.3:p.Ser443=
XM_011510158.1:c.768G>A	XP_011508460.1:p.Ser256=
NM_004767.4:c.1329G>A	NP_004758.3:p.Ser443=
XM_011510158.2:c.768G>A	XP_011508460.1:p.Ser256=
NM_004767.5:c.1329G>A MANE Select	NP_004758.3:p.Ser443=