Canonical Allele Identifier: CA462301620

Gene: INTS8

Linked Data

• MyVariant Identifiers: chr8:g.95840010T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.94827782T>G , CM000670.2:g.94827782T>G	GRCh38
NC_000008.10:g.95840010T>G , CM000670.1:g.95840010T>G	GRCh37
NC_000008.9:g.95909186T>G	NCBI36
NG_047163.1:g.19472T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523731.6:c.507T>G MANE Select	ENSP00000430338.1:p.Pro169=
ENST00000343161.8:c.507T>G	ENSP00000343274.4:p.Pro169=
ENST00000519053.5:c.180T>G	ENSP00000429056.1:p.Pro60=
ENST00000519457.5:c.366T>G	ENSP00000428260.1:p.Pro122=
ENST00000521860.5:c.469T>G
ENST00000522171.5:c.384T>G	ENSP00000429340.1:p.Pro128=
ENST00000523206.5:c.507T>G	ENSP00000429452.1:p.Pro169=
ENST00000523321.5:n.632T>G
ENST00000523731.5:c.507T>G	ENSP00000430338.1:p.Pro169=
ENST00000524333.5:c.507T>G	ENSP00000427840.1:p.Pro169=
NM_017864.3:c.507T>G	NP_060334.2:p.Pro169=
NR_073444.1:n.649T>G
NR_073445.1:n.649T>G
XM_006716602.2:c.507T>G	XP_006716665.1:p.Pro169=
XM_006716603.2:c.180T>G	XP_006716666.1:p.Pro60=
XM_011517155.1:c.384T>G	XP_011515457.1:p.Pro128=
XM_011517156.1:c.507T>G	XP_011515458.1:p.Pro169=
XM_011517157.1:c.180T>G	XP_011515459.1:p.Pro60=
XM_017013616.1:c.507T>G	XP_016869105.1:p.Pro169=
XM_017013617.1:c.507T>G	XP_016869106.1:p.Pro169=
XM_017013618.1:c.180T>G	XP_016869107.1:p.Pro60=
XM_017013619.1:c.-777T>G	XP_016869108.1:n.-777T>G
NM_017864.4:c.507T>G MANE Select	NP_060334.2:p.Pro169=
NR_073444.2:n.652T>G
NR_073445.2:n.652T>G