Canonical Allele Identifier: CA2561349584

Gene: CA8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192533_60192534insCTAGTGAGA , CM000670.2:g.60192533_60192534insCTAGTGAGA	GRCh38
NC_000008.10:g.61105092_61105093insCTAGTGAGA , CM000670.1:g.61105092_61105093insCTAGTGAGA	GRCh37
NC_000008.9:g.61267646_61267647insCTAGTGAGA	NCBI36
NG_023193.1:g.93862_93863insTCTCACTAG
NG_023193.2:g.93862_93863insTCTCACTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317995.5:c.*36-2549_*36-2548insTCTCACTAG MANE Select	ENSP00000314407.4:n.*36-2549_*36-2548insTCTCACTAG
ENST00000317995.4:c.*36-2549_*36-2548insTCTCACTAG	ENSP00000314407.4:n.*36-2549_*36-2548insTCTCACTAG
NM_004056.4:c.*36-2549_*36-2548insTCTCACTAG	NP_004047.3:n.*36-2549_*36-2548insTCTCACTAG
XM_011517586.1:c.*36-2549_*36-2548insTCTCACTAG	XP_011515888.1:n.*36-2549_*36-2548insTCTCACTAG
NM_001321839.1:c.*36-2549_*36-2548insTCTCACTAG	NP_001308768.1:n.*36-2549_*36-2548insTCTCACTAG
NM_004056.5:c.*36-2549_*36-2548insTCTCACTAG	NP_004047.3:n.*36-2549_*36-2548insTCTCACTAG
NR_135821.1:n.1235-2549_1235-2548insTCTCACTAG
XM_017013818.1:c.*36-2549_*36-2548insTCTCACTAG	XP_016869307.1:n.*36-2549_*36-2548insTCTCACTAG
NM_004056.6:c.*36-2549_*36-2548insTCTCACTAG MANE Select	NP_004047.3:n.*36-2549_*36-2548insTCTCACTAG
NM_001321839.2:c.*36-2549_*36-2548insTCTCACTAG	NP_001308768.1:n.*36-2549_*36-2548insTCTCACTAG
NR_135821.2:n.1212-2549_1212-2548insTCTCACTAG