Canonical Allele Identifier: CA422796452

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097495C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128367C>A , CM000663.2:g.202128367C>A	GRCh38
NC_000001.10:g.202097495C>A , CM000663.1:g.202097495C>A	GRCh37
NC_000001.9:g.200364118C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.838C>A
ENST00000682545.1:c.*263C>A	ENSP00000508402.1:n.*263C>A
ENST00000682887.1:c.1658C>A	ENSP00000506946.1:n.1658C>A
ENST00000683302.1:c.1188C>A	ENSP00000507885.1:p.Ile396=
ENST00000683557.1:c.*89C>A	ENSP00000508029.1:n.*89C>A
ENST00000367282.6:c.1257C>A MANE Select	ENSP00000356251.4:p.Ile419=
ENST00000367282.5:c.1257C>A	ENSP00000356251.4:p.Ile419=
NM_004767.3:c.1257C>A	NP_004758.3:p.Ile419=
XM_011510158.1:c.696C>A	XP_011508460.1:p.Ile232=
NM_004767.4:c.1257C>A	NP_004758.3:p.Ile419=
XM_011510158.2:c.696C>A	XP_011508460.1:p.Ile232=
NM_004767.5:c.1257C>A MANE Select	NP_004758.3:p.Ile419=