Canonical Allele Identifier: CA422796298

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097408C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128280C>G , CM000663.2:g.202128280C>G	GRCh38
NC_000001.10:g.202097408C>G , CM000663.1:g.202097408C>G	GRCh37
NC_000001.9:g.200364031C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.751C>G
ENST00000682545.1:c.*176C>G	ENSP00000508402.1:n.*176C>G
ENST00000682887.1:c.1571C>G	ENSP00000506946.1:n.1571C>G
ENST00000683302.1:c.1101C>G	ENSP00000507885.1:p.Thr367=
ENST00000683557.1:c.*2C>G	ENSP00000508029.1:n.*2C>G
ENST00000367282.6:c.1170C>G MANE Select	ENSP00000356251.4:p.Thr390=
ENST00000367282.5:c.1170C>G	ENSP00000356251.4:p.Thr390=
NM_004767.3:c.1170C>G	NP_004758.3:p.Thr390=
XM_011510158.1:c.609C>G	XP_011508460.1:p.Thr203=
NM_004767.4:c.1170C>G	NP_004758.3:p.Thr390=
XM_011510158.2:c.609C>G	XP_011508460.1:p.Thr203=
NM_004767.5:c.1170C>G MANE Select	NP_004758.3:p.Thr390=