Canonical Allele Identifier: CA344235746

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097363G>T (hg19) ; chr1:g.202128235G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128235G>T , CM000663.2:g.202128235G>T	GRCh38
NC_000001.10:g.202097363G>T , CM000663.1:g.202097363G>T	GRCh37
NC_000001.9:g.200363986G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.706G>T
ENST00000682545.1:c.*131G>T	ENSP00000508402.1:n.*131G>T
ENST00000682887.1:c.1526G>T	ENSP00000506946.1:n.1526G>T
ENST00000683302.1:c.1056G>T	ENSP00000507885.1:p.Glu352Asp
ENST00000683557.1:c.716G>T	ENSP00000508029.1:p.Arg239Ile
ENST00000367282.6:c.1125G>T MANE Select	ENSP00000356251.4:p.Glu375Asp
ENST00000367282.5:c.1125G>T	ENSP00000356251.4:p.Glu375Asp
NM_004767.3:c.1125G>T	NP_004758.3:p.Glu375Asp
XM_011510158.1:c.564G>T	XP_011508460.1:p.Glu188Asp
NM_004767.4:c.1125G>T	NP_004758.3:p.Glu375Asp
XM_011510158.2:c.564G>T	XP_011508460.1:p.Glu188Asp
NM_004767.5:c.1125G>T MANE Select	NP_004758.3:p.Glu375Asp