Canonical Allele Identifier: CA344236203

Gene: GPR37L1

Linked Data

• COSMIC: COSM3710507
• MyVariant Identifiers: chr1:g.202097575C>G (hg19) ; chr1:g.202128447C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128447C>G , CM000663.2:g.202128447C>G	GRCh38
NC_000001.10:g.202097575C>G , CM000663.1:g.202097575C>G	GRCh37
NC_000001.9:g.200364198C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.918C>G
ENST00000682545.1:c.*343C>G	ENSP00000508402.1:n.*343C>G
ENST00000682887.1:c.1738C>G	ENSP00000506946.1:n.1738C>G
ENST00000683302.1:c.1268C>G	ENSP00000507885.1:p.Ser423Cys
ENST00000683557.1:c.*169C>G	ENSP00000508029.1:n.*169C>G
ENST00000367282.6:c.1337C>G MANE Select	ENSP00000356251.4:p.Ser446Cys
ENST00000367282.5:c.1337C>G	ENSP00000356251.4:p.Ser446Cys
NM_004767.3:c.1337C>G	NP_004758.3:p.Ser446Cys
XM_011510158.1:c.776C>G	XP_011508460.1:p.Ser259Cys
NM_004767.4:c.1337C>G	NP_004758.3:p.Ser446Cys
XM_011510158.2:c.776C>G	XP_011508460.1:p.Ser259Cys
NM_004767.5:c.1337C>G MANE Select	NP_004758.3:p.Ser446Cys