Canonical Allele Identifier: CA35471460

Gene: GPR37L1

Linked Data

• dbSNP Id: rs945874015
• gnomAD v3: 1-202128332-A-G
• gnomAD v4: 1-202128332-A-G
• MyVariant Identifiers: chr1:g.202097460A>G (hg19) ; chr1:g.202128332A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128332A>G , CM000663.2:g.202128332A>G	GRCh38
NC_000001.10:g.202097460A>G , CM000663.1:g.202097460A>G	GRCh37
NC_000001.9:g.200364083A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.803A>G
ENST00000682545.1:c.*228A>G	ENSP00000508402.1:n.*228A>G
ENST00000682887.1:c.1623A>G	ENSP00000506946.1:n.1623A>G
ENST00000683302.1:c.1153A>G	ENSP00000507885.1:p.Lys385Glu
ENST00000683557.1:c.*54A>G	ENSP00000508029.1:n.*54A>G
ENST00000367282.6:c.1222A>G MANE Select	ENSP00000356251.4:p.Lys408Glu
ENST00000367282.5:c.1222A>G	ENSP00000356251.4:p.Lys408Glu
NM_004767.3:c.1222A>G	NP_004758.3:p.Lys408Glu
XM_011510158.1:c.661A>G	XP_011508460.1:p.Lys221Glu
NM_004767.4:c.1222A>G	NP_004758.3:p.Lys408Glu
XM_011510158.2:c.661A>G	XP_011508460.1:p.Lys221Glu
NM_004767.5:c.1222A>G MANE Select	NP_004758.3:p.Lys408Glu