Canonical Allele Identifier: CA422796393

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097465C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128337C>G , CM000663.2:g.202128337C>G	GRCh38
NC_000001.10:g.202097465C>G , CM000663.1:g.202097465C>G	GRCh37
NC_000001.9:g.200364088C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.808C>G
ENST00000682545.1:c.*233C>G	ENSP00000508402.1:n.*233C>G
ENST00000682887.1:c.1628C>G	ENSP00000506946.1:n.1628C>G
ENST00000683302.1:c.1158C>G	ENSP00000507885.1:p.Gly386=
ENST00000683557.1:c.*59C>G	ENSP00000508029.1:n.*59C>G
ENST00000367282.6:c.1227C>G MANE Select	ENSP00000356251.4:p.Gly409=
ENST00000367282.5:c.1227C>G	ENSP00000356251.4:p.Gly409=
NM_004767.3:c.1227C>G	NP_004758.3:p.Gly409=
XM_011510158.1:c.666C>G	XP_011508460.1:p.Gly222=
NM_004767.4:c.1227C>G	NP_004758.3:p.Gly409=
XM_011510158.2:c.666C>G	XP_011508460.1:p.Gly222=
NM_004767.5:c.1227C>G MANE Select	NP_004758.3:p.Gly409=