Canonical Allele Identifier: CA1803689114

Gene: INTS8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.94827774G= , CM000670.2:g.94827774G=	GRCh38
NC_000008.10:g.95840002G= , CM000670.1:g.95840002G=	GRCh37
NC_000008.9:g.95909178G=	NCBI36
NG_047163.1:g.19464G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523731.6:c.499G= MANE Select	ENSP00000430338.1:p.Gly167=
ENST00000343161.8:c.499G=	ENSP00000343274.4:p.Gly167=
ENST00000519053.5:c.172G=	ENSP00000429056.1:p.Gly58=
ENST00000519457.5:c.358G=	ENSP00000428260.1:p.Gly120=
ENST00000521860.5:c.461G=
ENST00000522171.5:c.376G=	ENSP00000429340.1:p.Gly126=
ENST00000523206.5:c.499G=	ENSP00000429452.1:p.Gly167=
ENST00000523321.5:n.624G=
ENST00000523731.5:c.499G=	ENSP00000430338.1:p.Gly167=
ENST00000524333.5:c.499G=	ENSP00000427840.1:p.Gly167=
NM_017864.3:c.499G=	NP_060334.2:p.Gly167=
NR_073444.1:n.641G=
NR_073445.1:n.641G=
XM_006716602.2:c.499G=	XP_006716665.1:p.Gly167=
XM_006716603.2:c.172G=	XP_006716666.1:p.Gly58=
XM_011517155.1:c.376G=	XP_011515457.1:p.Gly126=
XM_011517156.1:c.499G=	XP_011515458.1:p.Gly167=
XM_011517157.1:c.172G=	XP_011515459.1:p.Gly58=
XM_017013616.1:c.499G=	XP_016869105.1:p.Gly167=
XM_017013617.1:c.499G=	XP_016869106.1:p.Gly167=
XM_017013618.1:c.172G=	XP_016869107.1:p.Gly58=
XM_017013619.1:c.-785G=	XP_016869108.1:n.-785G=
NM_017864.4:c.499G= MANE Select	NP_060334.2:p.Gly167=
NR_073444.2:n.644G=
NR_073445.2:n.644G=