Canonical Allele Identifier: CA1787831933

Gene: CA8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192809_60192814delinsATTATT , CM000670.2:g.60192809_60192814delinsATTATT	GRCh38
NC_000008.10:g.61105368_61105373delinsATTATT , CM000670.1:g.61105368_61105373delinsATTATT	GRCh37
NC_000008.9:g.61267922_61267927delinsATTATT	NCBI36
NG_023193.1:g.93582_93587delinsAATAAT
NG_023193.2:g.93582_93587delinsAATAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317995.5:c.*36-2829_*36-2824delinsAATAAT MANE Select	ENSP00000314407.4:n.*36-2829_*36-2824delinsAATAAT
ENST00000317995.4:c.*36-2829_*36-2824delinsAATAAT	ENSP00000314407.4:n.*36-2829_*36-2824delinsAATAAT
NM_004056.4:c.*36-2829_*36-2824delinsAATAAT	NP_004047.3:n.*36-2829_*36-2824delinsAATAAT
XM_011517586.1:c.*36-2829_*36-2824delinsAATAAT	XP_011515888.1:n.*36-2829_*36-2824delinsAATAAT
NM_001321839.1:c.*36-2829_*36-2824delinsAATAAT	NP_001308768.1:n.*36-2829_*36-2824delinsAATAAT
NM_004056.5:c.*36-2829_*36-2824delinsAATAAT	NP_004047.3:n.*36-2829_*36-2824delinsAATAAT
NR_135821.1:n.1235-2829_1235-2824delinsAATAAT
XM_017013818.1:c.*36-2829_*36-2824delinsAATAAT	XP_016869307.1:n.*36-2829_*36-2824delinsAATAAT
NM_004056.6:c.*36-2829_*36-2824delinsAATAAT MANE Select	NP_004047.3:n.*36-2829_*36-2824delinsAATAAT
NM_001321839.2:c.*36-2829_*36-2824delinsAATAAT	NP_001308768.1:n.*36-2829_*36-2824delinsAATAAT
NR_135821.2:n.1212-2829_1212-2824delinsAATAAT