Canonical Allele Identifier: CA369196959

Gene: GARIN1B

Linked Data

• MyVariant Identifiers: chr7:g.128363349C>A (hg19) ; chr7:g.128723295C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128723295C>A , CM000669.2:g.128723295C>A	GRCh38
NC_000007.13:g.128363349C>A , CM000669.1:g.128363349C>A	GRCh37
NC_000007.12:g.128150585C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621392.5:c.786C>A MANE Select	ENSP00000477573.2:p.Asp262Glu
ENST00000315184.9:c.786C>A	ENSP00000326652.4:p.Asp262Glu
ENST00000466842.1:c.354C>A	ENSP00000417930.1:p.Asp118Glu
ENST00000469348.5:n.645C>A
ENST00000471558.5:c.786C>A	ENSP00000418672.1:p.Asp262Glu
ENST00000484425.6:c.357C>A	ENSP00000418591.2:p.Asp119Glu
ENST00000485070.5:c.489C>A	ENSP00000418192.1:p.Asp163Glu
ENST00000493738.5:n.742C>A
ENST00000621392.4:c.489C>A	ENSP00000477573.1:p.Asp163Glu
NM_001282788.1:c.786C>A	NP_001269717.1:p.Asp262Glu
NM_001282789.1:c.489C>A	NP_001269718.1:p.Asp163Glu
NM_032599.3:c.786C>A	NP_115988.1:p.Asp262Glu
NR_104242.1:n.886C>A
NR_104243.1:n.775C>A
XM_017012743.2:c.786C>A	XP_016868232.1:p.Asp262Glu
XR_002956499.1:n.837C>A
NM_001282788.2:c.786C>A	NP_001269717.1:p.Asp262Glu
NM_001282789.2:c.489C>A	NP_001269718.1:p.Asp163Glu
NM_032599.4:c.786C>A	NP_115988.1:p.Asp262Glu
NR_104242.2:n.837C>A
NR_104243.2:n.775C>A
NM_001282788.3:c.786C>A MANE Select	NP_001269717.1:p.Asp262Glu