Canonical Allele Identifier: CA1803689015

Gene: INTS8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.94827732A= , CM000670.2:g.94827732A=	GRCh38
NC_000008.10:g.95839960A= , CM000670.1:g.95839960A=	GRCh37
NC_000008.9:g.95909136A=	NCBI36
NG_047163.1:g.19422A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523731.6:c.457A= MANE Select	ENSP00000430338.1:p.Thr153=
ENST00000343161.8:c.457A=	ENSP00000343274.4:p.Thr153=
ENST00000519053.5:c.130A=	ENSP00000429056.1:p.Thr44=
ENST00000519457.5:c.316A=	ENSP00000428260.1:p.Thr106=
ENST00000521860.5:c.419A=
ENST00000522171.5:c.334A=	ENSP00000429340.1:p.Thr112=
ENST00000523206.5:c.457A=	ENSP00000429452.1:p.Thr153=
ENST00000523321.5:n.582A=
ENST00000523731.5:c.457A=	ENSP00000430338.1:p.Thr153=
ENST00000524333.5:c.457A=	ENSP00000427840.1:p.Thr153=
NM_017864.3:c.457A=	NP_060334.2:p.Thr153=
NR_073444.1:n.599A=
NR_073445.1:n.599A=
XM_006716602.2:c.457A=	XP_006716665.1:p.Thr153=
XM_006716603.2:c.130A=	XP_006716666.1:p.Thr44=
XM_011517155.1:c.334A=	XP_011515457.1:p.Thr112=
XM_011517156.1:c.457A=	XP_011515458.1:p.Thr153=
XM_011517157.1:c.130A=	XP_011515459.1:p.Thr44=
XM_017013616.1:c.457A=	XP_016869105.1:p.Thr153=
XM_017013617.1:c.457A=	XP_016869106.1:p.Thr153=
XM_017013618.1:c.130A=	XP_016869107.1:p.Thr44=
XM_017013619.1:c.-827A=	XP_016869108.1:n.-827A=
NM_017864.4:c.457A= MANE Select	NP_060334.2:p.Thr153=
NR_073444.2:n.602A=
NR_073445.2:n.602A=