Canonical Allele Identifier: CA853842492

Gene: CA8

Linked Data

• dbSNP Id: rs1205309099
• MyVariant Identifiers: chr8:g.61105369_61105370insA (hg19) ; chr8:g.60192810_60192811insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192810_60192811insA , CM000670.2:g.60192810_60192811insA	GRCh38
NC_000008.10:g.61105369_61105370insA , CM000670.1:g.61105369_61105370insA	GRCh37
NC_000008.9:g.61267923_61267924insA	NCBI36
NG_023193.1:g.93585_93586insT
NG_023193.2:g.93585_93586insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317995.5:c.*36-2826_*36-2825insT MANE Select	ENSP00000314407.4:n.*36-2826_*36-2825insT
ENST00000317995.4:c.*36-2826_*36-2825insT	ENSP00000314407.4:n.*36-2826_*36-2825insT
NM_004056.4:c.*36-2826_*36-2825insT	NP_004047.3:n.*36-2826_*36-2825insT
XM_011517586.1:c.*36-2826_*36-2825insT	XP_011515888.1:n.*36-2826_*36-2825insT
NM_001321839.1:c.*36-2826_*36-2825insT	NP_001308768.1:n.*36-2826_*36-2825insT
NM_004056.5:c.*36-2826_*36-2825insT	NP_004047.3:n.*36-2826_*36-2825insT
NR_135821.1:n.1235-2826_1235-2825insT
XM_017013818.1:c.*36-2826_*36-2825insT	XP_016869307.1:n.*36-2826_*36-2825insT
NM_004056.6:c.*36-2826_*36-2825insT MANE Select	NP_004047.3:n.*36-2826_*36-2825insT
NM_001321839.2:c.*36-2826_*36-2825insT	NP_001308768.1:n.*36-2826_*36-2825insT
NR_135821.2:n.1212-2826_1212-2825insT