Canonical Allele Identifier: CA344235962

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097467C>G (hg19) ; chr1:g.202128339C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128339C>G , CM000663.2:g.202128339C>G	GRCh38
NC_000001.10:g.202097467C>G , CM000663.1:g.202097467C>G	GRCh37
NC_000001.9:g.200364090C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.810C>G
ENST00000682545.1:c.*235C>G	ENSP00000508402.1:n.*235C>G
ENST00000682887.1:c.1630C>G	ENSP00000506946.1:n.1630C>G
ENST00000683302.1:c.1160C>G	ENSP00000507885.1:p.Ala387Gly
ENST00000683557.1:c.*61C>G	ENSP00000508029.1:n.*61C>G
ENST00000367282.6:c.1229C>G MANE Select	ENSP00000356251.4:p.Ala410Gly
ENST00000367282.5:c.1229C>G	ENSP00000356251.4:p.Ala410Gly
NM_004767.3:c.1229C>G	NP_004758.3:p.Ala410Gly
XM_011510158.1:c.668C>G	XP_011508460.1:p.Ala223Gly
NM_004767.4:c.1229C>G	NP_004758.3:p.Ala410Gly
XM_011510158.2:c.668C>G	XP_011508460.1:p.Ala223Gly
NM_004767.5:c.1229C>G MANE Select	NP_004758.3:p.Ala410Gly