Canonical Allele Identifier: CA1787831588
Gene: CA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192560_60192564delinsAAAGT , CM000670.2:g.60192560_60192564delinsAAAGT GRCh38
NC_000008.10:g.61105119_61105123delinsAAAGT , CM000670.1:g.61105119_61105123delinsAAAGT GRCh37
NC_000008.9:g.61267673_61267677delinsAAAGT NCBI36
NG_023193.1:g.93832_93836delinsACTTT
NG_023193.2:g.93832_93836delinsACTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000317995.5:c.*36-2579_*36-2575delinsACTTT MANE Select ENSP00000314407.4:n.*36-2579_*36-2575deli...
ENST00000317995.4:c.*36-2579_*36-2575delinsACTTT ENSP00000314407.4:n.*36-2579_*36-2575deli...
NM_004056.4:c.*36-2579_*36-2575delinsACTTT NP_004047.3:n.*36-2579_*36-2575delinsACTT...
XM_011517586.1:c.*36-2579_*36-2575delinsACTTT XP_011515888.1:n.*36-2579_*36-2575delinsA...
NM_001321839.1:c.*36-2579_*36-2575delinsACTTT NP_001308768.1:n.*36-2579_*36-2575delinsA...
NM_004056.5:c.*36-2579_*36-2575delinsACTTT NP_004047.3:n.*36-2579_*36-2575delinsACTT...
NR_135821.1:n.1235-2579_1235-2575delinsACTTT
XM_017013818.1:c.*36-2579_*36-2575delinsACTTT XP_016869307.1:n.*36-2579_*36-2575delinsA...
NM_004056.6:c.*36-2579_*36-2575delinsACTTT MANE Select NP_004047.3:n.*36-2579_*36-2575delinsACTT...
NM_001321839.2:c.*36-2579_*36-2575delinsACTTT NP_001308768.1:n.*36-2579_*36-2575delinsA...
NR_135821.2:n.1212-2579_1212-2575delinsACTTT