Canonical Allele Identifier: CA344236096

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097531C>G (hg19) ; chr1:g.202128403C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128403C>G , CM000663.2:g.202128403C>G	GRCh38
NC_000001.10:g.202097531C>G , CM000663.1:g.202097531C>G	GRCh37
NC_000001.9:g.200364154C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.874C>G
ENST00000682545.1:c.*299C>G	ENSP00000508402.1:n.*299C>G
ENST00000682887.1:c.1694C>G	ENSP00000506946.1:n.1694C>G
ENST00000683302.1:c.1224C>G	ENSP00000507885.1:p.Cys408Trp
ENST00000683557.1:c.*125C>G	ENSP00000508029.1:n.*125C>G
ENST00000367282.6:c.1293C>G MANE Select	ENSP00000356251.4:p.Cys431Trp
ENST00000367282.5:c.1293C>G	ENSP00000356251.4:p.Cys431Trp
NM_004767.3:c.1293C>G	NP_004758.3:p.Cys431Trp
XM_011510158.1:c.732C>G	XP_011508460.1:p.Cys244Trp
NM_004767.4:c.1293C>G	NP_004758.3:p.Cys431Trp
XM_011510158.2:c.732C>G	XP_011508460.1:p.Cys244Trp
NM_004767.5:c.1293C>G MANE Select	NP_004758.3:p.Cys431Trp