Canonical Allele Identifier: CA1787831830
Gene: CA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192739_60192741delinsGTT , CM000670.2:g.60192739_60192741delinsGTT GRCh38
NC_000008.10:g.61105298_61105300delinsGTT , CM000670.1:g.61105298_61105300delinsGTT GRCh37
NC_000008.9:g.61267852_61267854delinsGTT NCBI36
NG_023193.1:g.93655_93657delinsAAC
NG_023193.2:g.93655_93657delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000317995.5:c.*36-2756_*36-2754delinsAAC MANE Select ENSP00000314407.4:n.*36-2756_*36-2754delinsAAC
ENST00000317995.4:c.*36-2756_*36-2754delinsAAC ENSP00000314407.4:n.*36-2756_*36-2754delinsAAC
NM_004056.4:c.*36-2756_*36-2754delinsAAC NP_004047.3:n.*36-2756_*36-2754delinsAAC
XM_011517586.1:c.*36-2756_*36-2754delinsAAC XP_011515888.1:n.*36-2756_*36-2754delinsAAC
NM_001321839.1:c.*36-2756_*36-2754delinsAAC NP_001308768.1:n.*36-2756_*36-2754delinsAAC
NM_004056.5:c.*36-2756_*36-2754delinsAAC NP_004047.3:n.*36-2756_*36-2754delinsAAC
NR_135821.1:n.1235-2756_1235-2754delinsAAC
XM_017013818.1:c.*36-2756_*36-2754delinsAAC XP_016869307.1:n.*36-2756_*36-2754delinsAAC
NM_004056.6:c.*36-2756_*36-2754delinsAAC MANE Select NP_004047.3:n.*36-2756_*36-2754delinsAAC
NM_001321839.2:c.*36-2756_*36-2754delinsAAC NP_001308768.1:n.*36-2756_*36-2754delinsAAC
NR_135821.2:n.1212-2756_1212-2754delinsAAC