Canonical Allele Identifier: CA853842332

Gene: CA8

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192458_60192459insGCTAAAAAA , CM000670.2:g.60192458_60192459insGCTAAAAAA	GRCh38
NC_000008.10:g.61105017_61105018insGCTAAAAAA , CM000670.1:g.61105017_61105018insGCTAAAAAA	GRCh37
NC_000008.9:g.61267571_61267572insGCTAAAAAA	NCBI36
NG_023193.1:g.93938_93939insTTTTTAGCT
NG_023193.2:g.93938_93939insTTTTTAGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317995.5:c.*36-2473_*36-2472insTTTTTAGCT MANE Select	ENSP00000314407.4:n.*36-2473_*36-2472insTTTTTAGCT
ENST00000317995.4:c.*36-2473_*36-2472insTTTTTAGCT	ENSP00000314407.4:n.*36-2473_*36-2472insTTTTTAGCT
NM_004056.4:c.*36-2473_*36-2472insTTTTTAGCT	NP_004047.3:n.*36-2473_*36-2472insTTTTTAGCT
XM_011517586.1:c.*36-2473_*36-2472insTTTTTAGCT	XP_011515888.1:n.*36-2473_*36-2472insTTTTTAGCT
NM_001321839.1:c.*36-2473_*36-2472insTTTTTAGCT	NP_001308768.1:n.*36-2473_*36-2472insTTTTTAGCT
NM_004056.5:c.*36-2473_*36-2472insTTTTTAGCT	NP_004047.3:n.*36-2473_*36-2472insTTTTTAGCT
NR_135821.1:n.1235-2473_1235-2472insTTTTTAGCT
XM_017013818.1:c.*36-2473_*36-2472insTTTTTAGCT	XP_016869307.1:n.*36-2473_*36-2472insTTTTTAGCT
NM_004056.6:c.*36-2473_*36-2472insTTTTTAGCT MANE Select	NP_004047.3:n.*36-2473_*36-2472insTTTTTAGCT
NM_001321839.2:c.*36-2473_*36-2472insTTTTTAGCT	NP_001308768.1:n.*36-2473_*36-2472insTTTTTAGCT
NR_135821.2:n.1212-2473_1212-2472insTTTTTAGCT