Canonical Allele Identifier: CA1330220

Gene: GPR37L1

Linked Data

• dbSNP Id: rs761506972
• ExAC: 1:202097551 A / G
• gnomAD v2: 1-202097551-A-G
• gnomAD v4: 1-202128423-A-G
• MyVariant Identifiers: chr1:g.202097551A>G (hg19) ; chr1:g.202128423A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128423A>G , CM000663.2:g.202128423A>G	GRCh38
NC_000001.10:g.202097551A>G , CM000663.1:g.202097551A>G	GRCh37
NC_000001.9:g.200364174A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.894A>G
ENST00000682545.1:c.*319A>G	ENSP00000508402.1:n.*319A>G
ENST00000682887.1:c.1714A>G	ENSP00000506946.1:n.1714A>G
ENST00000683302.1:c.1244A>G	ENSP00000507885.1:p.Glu415Gly
ENST00000683557.1:c.*145A>G	ENSP00000508029.1:n.*145A>G
ENST00000367282.6:c.1313A>G MANE Select	ENSP00000356251.4:p.Glu438Gly
ENST00000367282.5:c.1313A>G	ENSP00000356251.4:p.Glu438Gly
NM_004767.3:c.1313A>G	NP_004758.3:p.Glu438Gly
XM_011510158.1:c.752A>G	XP_011508460.1:p.Glu251Gly
NM_004767.4:c.1313A>G	NP_004758.3:p.Glu438Gly
XM_011510158.2:c.752A>G	XP_011508460.1:p.Glu251Gly
NM_004767.5:c.1313A>G MANE Select	NP_004758.3:p.Glu438Gly