Canonical Allele Identifier: CA344236176

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097563C>A (hg19) ; chr1:g.202128435C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128435C>A , CM000663.2:g.202128435C>A	GRCh38
NC_000001.10:g.202097563C>A , CM000663.1:g.202097563C>A	GRCh37
NC_000001.9:g.200364186C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.906C>A
ENST00000682545.1:c.*331C>A	ENSP00000508402.1:n.*331C>A
ENST00000682887.1:c.1726C>A	ENSP00000506946.1:n.1726C>A
ENST00000683302.1:c.1256C>A	ENSP00000507885.1:p.Ala419Asp
ENST00000683557.1:c.*157C>A	ENSP00000508029.1:n.*157C>A
ENST00000367282.6:c.1325C>A MANE Select	ENSP00000356251.4:p.Ala442Asp
ENST00000367282.5:c.1325C>A	ENSP00000356251.4:p.Ala442Asp
NM_004767.3:c.1325C>A	NP_004758.3:p.Ala442Asp
XM_011510158.1:c.764C>A	XP_011508460.1:p.Ala255Asp
NM_004767.4:c.1325C>A	NP_004758.3:p.Ala442Asp
XM_011510158.2:c.764C>A	XP_011508460.1:p.Ala255Asp
NM_004767.5:c.1325C>A MANE Select	NP_004758.3:p.Ala442Asp