Canonical Allele Identifier: CA462301411

Gene: INTS8

Linked Data

• MyVariant Identifiers: chr8:g.95839992G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.94827764G>A , CM000670.2:g.94827764G>A	GRCh38
NC_000008.10:g.95839992G>A , CM000670.1:g.95839992G>A	GRCh37
NC_000008.9:g.95909168G>A	NCBI36
NG_047163.1:g.19454G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523731.6:c.489G>A MANE Select	ENSP00000430338.1:p.Gln163=
ENST00000343161.8:c.489G>A	ENSP00000343274.4:p.Gln163=
ENST00000519053.5:c.162G>A	ENSP00000429056.1:p.Gln54=
ENST00000519457.5:c.348G>A	ENSP00000428260.1:p.Gln116=
ENST00000521860.5:c.451G>A
ENST00000522171.5:c.366G>A	ENSP00000429340.1:p.Gln122=
ENST00000523206.5:c.489G>A	ENSP00000429452.1:p.Gln163=
ENST00000523321.5:n.614G>A
ENST00000523731.5:c.489G>A	ENSP00000430338.1:p.Gln163=
ENST00000524333.5:c.489G>A	ENSP00000427840.1:p.Gln163=
NM_017864.3:c.489G>A	NP_060334.2:p.Gln163=
NR_073444.1:n.631G>A
NR_073445.1:n.631G>A
XM_006716602.2:c.489G>A	XP_006716665.1:p.Gln163=
XM_006716603.2:c.162G>A	XP_006716666.1:p.Gln54=
XM_011517155.1:c.366G>A	XP_011515457.1:p.Gln122=
XM_011517156.1:c.489G>A	XP_011515458.1:p.Gln163=
XM_011517157.1:c.162G>A	XP_011515459.1:p.Gln54=
XM_017013616.1:c.489G>A	XP_016869105.1:p.Gln163=
XM_017013617.1:c.489G>A	XP_016869106.1:p.Gln163=
XM_017013618.1:c.162G>A	XP_016869107.1:p.Gln54=
XM_017013619.1:c.-795G>A	XP_016869108.1:n.-795G>A
NM_017864.4:c.489G>A MANE Select	NP_060334.2:p.Gln163=
NR_073444.2:n.634G>A
NR_073445.2:n.634G>A