Canonical Allele Identifier: CA1787831906
Gene: CA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192791_60192794delinsCCTT , CM000670.2:g.60192791_60192794delinsCCTT GRCh38
NC_000008.10:g.61105350_61105353delinsCCTT , CM000670.1:g.61105350_61105353delinsCCTT GRCh37
NC_000008.9:g.61267904_61267907delinsCCTT NCBI36
NG_023193.1:g.93602_93605delinsAAGG
NG_023193.2:g.93602_93605delinsAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000317995.5:c.*36-2809_*36-2806delinsAAGG MANE Select ENSP00000314407.4:n.*36-2809_*36-2806delinsAAGG
ENST00000317995.4:c.*36-2809_*36-2806delinsAAGG ENSP00000314407.4:n.*36-2809_*36-2806delinsAAGG
NM_004056.4:c.*36-2809_*36-2806delinsAAGG NP_004047.3:n.*36-2809_*36-2806delinsAAGG
XM_011517586.1:c.*36-2809_*36-2806delinsAAGG XP_011515888.1:n.*36-2809_*36-2806delinsAAGG
NM_001321839.1:c.*36-2809_*36-2806delinsAAGG NP_001308768.1:n.*36-2809_*36-2806delinsAAGG
NM_004056.5:c.*36-2809_*36-2806delinsAAGG NP_004047.3:n.*36-2809_*36-2806delinsAAGG
NR_135821.1:n.1235-2809_1235-2806delinsAAGG
XM_017013818.1:c.*36-2809_*36-2806delinsAAGG XP_016869307.1:n.*36-2809_*36-2806delinsAAGG
NM_004056.6:c.*36-2809_*36-2806delinsAAGG MANE Select NP_004047.3:n.*36-2809_*36-2806delinsAAGG
NM_001321839.2:c.*36-2809_*36-2806delinsAAGG NP_001308768.1:n.*36-2809_*36-2806delinsAAGG
NR_135821.2:n.1212-2809_1212-2806delinsAAGG