Canonical Allele Identifier: CA422796344

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097435C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128307C>G , CM000663.2:g.202128307C>G	GRCh38
NC_000001.10:g.202097435C>G , CM000663.1:g.202097435C>G	GRCh37
NC_000001.9:g.200364058C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.778C>G
ENST00000682545.1:c.*203C>G	ENSP00000508402.1:n.*203C>G
ENST00000682887.1:c.1598C>G	ENSP00000506946.1:n.1598C>G
ENST00000683302.1:c.1128C>G	ENSP00000507885.1:p.Leu376=
ENST00000683557.1:c.*29C>G	ENSP00000508029.1:n.*29C>G
ENST00000367282.6:c.1197C>G MANE Select	ENSP00000356251.4:p.Leu399=
ENST00000367282.5:c.1197C>G	ENSP00000356251.4:p.Leu399=
NM_004767.3:c.1197C>G	NP_004758.3:p.Leu399=
XM_011510158.1:c.636C>G	XP_011508460.1:p.Leu212=
NM_004767.4:c.1197C>G	NP_004758.3:p.Leu399=
XM_011510158.2:c.636C>G	XP_011508460.1:p.Leu212=
NM_004767.5:c.1197C>G MANE Select	NP_004758.3:p.Leu399=