Canonical Allele Identifier: CA422796439

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097486C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128358C>G , CM000663.2:g.202128358C>G	GRCh38
NC_000001.10:g.202097486C>G , CM000663.1:g.202097486C>G	GRCh37
NC_000001.9:g.200364109C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.829C>G
ENST00000682545.1:c.*254C>G	ENSP00000508402.1:n.*254C>G
ENST00000682887.1:c.1649C>G	ENSP00000506946.1:n.1649C>G
ENST00000683302.1:c.1179C>G	ENSP00000507885.1:p.Leu393=
ENST00000683557.1:c.*80C>G	ENSP00000508029.1:n.*80C>G
ENST00000367282.6:c.1248C>G MANE Select	ENSP00000356251.4:p.Leu416=
ENST00000367282.5:c.1248C>G	ENSP00000356251.4:p.Leu416=
NM_004767.3:c.1248C>G	NP_004758.3:p.Leu416=
XM_011510158.1:c.687C>G	XP_011508460.1:p.Leu229=
NM_004767.4:c.1248C>G	NP_004758.3:p.Leu416=
XM_011510158.2:c.687C>G	XP_011508460.1:p.Leu229=
NM_004767.5:c.1248C>G MANE Select	NP_004758.3:p.Leu416=