Canonical Allele Identifier: CA371732006
Gene: INTS8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.94827789A>G , CM000670.2:g.94827789A>G GRCh38
NC_000008.10:g.95840017A>G , CM000670.1:g.95840017A>G GRCh37
NC_000008.9:g.95909193A>G NCBI36
NG_047163.1:g.19479A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000523731.6:c.514A>G MANE Select ENSP00000430338.1:p.Ser172Gly
ENST00000343161.8:c.514A>G ENSP00000343274.4:p.Ser172Gly
ENST00000519053.5:c.187A>G ENSP00000429056.1:p.Ser63Gly
ENST00000519457.5:c.373A>G ENSP00000428260.1:p.Ser125Gly
ENST00000521860.5:c.476A>G
ENST00000522171.5:c.391A>G ENSP00000429340.1:p.Ser131Gly
ENST00000523206.5:c.514A>G ENSP00000429452.1:p.Ser172Gly
ENST00000523321.5:n.639A>G
ENST00000523731.5:c.514A>G ENSP00000430338.1:p.Ser172Gly
ENST00000524333.5:c.514A>G ENSP00000427840.1:p.Ser172Gly
NM_017864.3:c.514A>G NP_060334.2:p.Ser172Gly
NR_073444.1:n.656A>G
NR_073445.1:n.656A>G
XM_006716602.2:c.514A>G XP_006716665.1:p.Ser172Gly
XM_006716603.2:c.187A>G XP_006716666.1:p.Ser63Gly
XM_011517155.1:c.391A>G XP_011515457.1:p.Ser131Gly
XM_011517156.1:c.514A>G XP_011515458.1:p.Ser172Gly
XM_011517157.1:c.187A>G XP_011515459.1:p.Ser63Gly
XM_017013616.1:c.514A>G XP_016869105.1:p.Ser172Gly
XM_017013617.1:c.514A>G XP_016869106.1:p.Ser172Gly
XM_017013618.1:c.187A>G XP_016869107.1:p.Ser63Gly
XM_017013619.1:c.-770A>G XP_016869108.1:n.-770A>G
NM_017864.4:c.514A>G MANE Select NP_060334.2:p.Ser172Gly
NR_073444.2:n.659A>G
NR_073445.2:n.659A>G