Canonical Allele Identifier: CA853842365

Gene: CA8

Linked Data

• dbSNP Id: rs1383112986
• MyVariant Identifiers: chr8:g.61105103_61105104del (hg19) ; chr8:g.60192544_60192545del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192545_60192546del , CM000670.2:g.60192545_60192546del	GRCh38
NC_000008.10:g.61105104_61105105del , CM000670.1:g.61105104_61105105del	GRCh37
NC_000008.9:g.61267658_61267659del	NCBI36
NG_023193.1:g.93851_93852del
NG_023193.2:g.93851_93852del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317995.5:c.*36-2560_*36-2559del MANE Select	ENSP00000314407.4:n.*36-2560_*36-2559del
ENST00000317995.4:c.*36-2560_*36-2559del	ENSP00000314407.4:n.*36-2560_*36-2559del
NM_004056.4:c.*36-2560_*36-2559del	NP_004047.3:n.*36-2560_*36-2559del
XM_011517586.1:c.*36-2560_*36-2559del	XP_011515888.1:n.*36-2560_*36-2559del
NM_001321839.1:c.*36-2560_*36-2559del	NP_001308768.1:n.*36-2560_*36-2559del
NM_004056.5:c.*36-2560_*36-2559del	NP_004047.3:n.*36-2560_*36-2559del
NR_135821.1:n.1235-2560_1235-2559del
XM_017013818.1:c.*36-2560_*36-2559del	XP_016869307.1:n.*36-2560_*36-2559del
NM_004056.6:c.*36-2560_*36-2559del MANE Select	NP_004047.3:n.*36-2560_*36-2559del
NM_001321839.2:c.*36-2560_*36-2559del	NP_001308768.1:n.*36-2560_*36-2559del
NR_135821.2:n.1212-2560_1212-2559del