Canonical Allele Identifier: CA1803689031

Gene: INTS8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.94827744_94827745delinsAG , CM000670.2:g.94827744_94827745delinsAG	GRCh38
NC_000008.10:g.95839972_95839973delinsAG , CM000670.1:g.95839972_95839973delinsAG	GRCh37
NC_000008.9:g.95909148_95909149delinsAG	NCBI36
NG_047163.1:g.19434_19435delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523731.6:c.469_470delinsAG MANE Select	ENSP00000430338.1:p.Ser157=
ENST00000343161.8:c.469_470delinsAG	ENSP00000343274.4:p.Ser157=
ENST00000519053.5:c.142_143delinsAG	ENSP00000429056.1:p.Ser48=
ENST00000519457.5:c.328_329delinsAG	ENSP00000428260.1:p.Ser110=
ENST00000521860.5:c.431_432delinsAG
ENST00000522171.5:c.346_347delinsAG	ENSP00000429340.1:p.Ser116=
ENST00000523206.5:c.469_470delinsAG	ENSP00000429452.1:p.Ser157=
ENST00000523321.5:n.594_595delinsAG
ENST00000523731.5:c.469_470delinsAG	ENSP00000430338.1:p.Ser157=
ENST00000524333.5:c.469_470delinsAG	ENSP00000427840.1:p.Ser157=
NM_017864.3:c.469_470delinsAG	NP_060334.2:p.Ser157=
NR_073444.1:n.611_612delinsAG
NR_073445.1:n.611_612delinsAG
XM_006716602.2:c.469_470delinsAG	XP_006716665.1:p.Ser157=
XM_006716603.2:c.142_143delinsAG	XP_006716666.1:p.Ser48=
XM_011517155.1:c.346_347delinsAG	XP_011515457.1:p.Ser116=
XM_011517156.1:c.469_470delinsAG	XP_011515458.1:p.Ser157=
XM_011517157.1:c.142_143delinsAG	XP_011515459.1:p.Ser48=
XM_017013616.1:c.469_470delinsAG	XP_016869105.1:p.Ser157=
XM_017013617.1:c.469_470delinsAG	XP_016869106.1:p.Ser157=
XM_017013618.1:c.142_143delinsAG	XP_016869107.1:p.Ser48=
XM_017013619.1:c.-815_-814delinsAG	XP_016869108.1:n.-815_-814delinsAG
NM_017864.4:c.469_470delinsAG MANE Select	NP_060334.2:p.Ser157=
NR_073444.2:n.614_615delinsAG
NR_073445.2:n.614_615delinsAG