Canonical Allele Identifier: CA422796421

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1654735290
• gnomAD v4: 1-202128349-A-G
• MyVariant Identifiers: chr1:g.202097477A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128349A>G , CM000663.2:g.202128349A>G	GRCh38
NC_000001.10:g.202097477A>G , CM000663.1:g.202097477A>G	GRCh37
NC_000001.9:g.200364100A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.820A>G
ENST00000682545.1:c.*245A>G	ENSP00000508402.1:n.*245A>G
ENST00000682887.1:c.1640A>G	ENSP00000506946.1:n.1640A>G
ENST00000683302.1:c.1170A>G	ENSP00000507885.1:p.Pro390=
ENST00000683557.1:c.*71A>G	ENSP00000508029.1:n.*71A>G
ENST00000367282.6:c.1239A>G MANE Select	ENSP00000356251.4:p.Pro413=
ENST00000367282.5:c.1239A>G	ENSP00000356251.4:p.Pro413=
NM_004767.3:c.1239A>G	NP_004758.3:p.Pro413=
XM_011510158.1:c.678A>G	XP_011508460.1:p.Pro226=
NM_004767.4:c.1239A>G	NP_004758.3:p.Pro413=
XM_011510158.2:c.678A>G	XP_011508460.1:p.Pro226=
NM_004767.5:c.1239A>G MANE Select	NP_004758.3:p.Pro413=