Canonical Allele Identifier: CA1803689677

Gene: INTS8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.94828066_94828070delinsGACTC , CM000670.2:g.94828066_94828070delinsGACTC	GRCh38
NC_000008.10:g.95840294_95840298delinsGACTC , CM000670.1:g.95840294_95840298delinsGACTC	GRCh37
NC_000008.9:g.95909470_95909474delinsGACTC	NCBI36
NG_047163.1:g.19756_19760delinsGACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523731.6:c.518+273_518+277delinsGACTC MANE Select	ENSP00000430338.1:n.518+273_518+277delinsGACTC
ENST00000343161.8:c.518+273_518+277delinsGACTC	ENSP00000343274.4:n.518+273_518+277delinsGACTC
ENST00000519053.5:c.191+273_191+277delinsGACTC	ENSP00000429056.1:n.191+273_191+277delinsGACTC
ENST00000519457.5:c.377+273_377+277delinsGACTC	ENSP00000428260.1:n.377+273_377+277delinsGACTC
ENST00000521860.5:c.480+273_480+277delinsGACTC
ENST00000522171.5:c.395+273_395+277delinsGACTC	ENSP00000429340.1:n.395+273_395+277delinsGACTC
ENST00000523206.5:c.518+273_518+277delinsGACTC	ENSP00000429452.1:n.518+273_518+277delinsGACTC
ENST00000523321.5:n.643+273_643+277delinsGACTC
ENST00000523731.5:c.518+273_518+277delinsGACTC	ENSP00000430338.1:n.518+273_518+277delinsGACTC
ENST00000524333.5:c.518+273_518+277delinsGACTC	ENSP00000427840.1:n.518+273_518+277delinsGACTC
NM_017864.3:c.518+273_518+277delinsGACTC	NP_060334.2:n.518+273_518+277delinsGACTC
NR_073444.1:n.660+273_660+277delinsGACTC
NR_073445.1:n.660+273_660+277delinsGACTC
XM_006716602.2:c.518+273_518+277delinsGACTC	XP_006716665.1:n.518+273_518+277delinsGACTC
XM_006716603.2:c.191+273_191+277delinsGACTC	XP_006716666.1:n.191+273_191+277delinsGACTC
XM_011517155.1:c.395+273_395+277delinsGACTC	XP_011515457.1:n.395+273_395+277delinsGACTC
XM_011517156.1:c.518+273_518+277delinsGACTC	XP_011515458.1:n.518+273_518+277delinsGACTC
XM_011517157.1:c.191+273_191+277delinsGACTC	XP_011515459.1:n.191+273_191+277delinsGACTC
XM_017013616.1:c.518+273_518+277delinsGACTC	XP_016869105.1:n.518+273_518+277delinsGACTC
XM_017013617.1:c.518+273_518+277delinsGACTC	XP_016869106.1:n.518+273_518+277delinsGACTC
XM_017013618.1:c.191+273_191+277delinsGACTC	XP_016869107.1:n.191+273_191+277delinsGACTC
XM_017013619.1:c.-766+273_-766+277delinsGACTC	XP_016869108.1:n.-766+273_-766+277delinsGACTC
NM_017864.4:c.518+273_518+277delinsGACTC MANE Select	NP_060334.2:n.518+273_518+277delinsGACTC
NR_073444.2:n.663+273_663+277delinsGACTC
NR_073445.2:n.663+273_663+277delinsGACTC