Canonical Allele Identifier: CA1787831629

Gene: CA8

Linked Data

• dbSNP Id: rs1806161405

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192592C>G , CM000670.2:g.60192592C>G	GRCh38
NC_000008.10:g.61105151C>G , CM000670.1:g.61105151C>G	GRCh37
NC_000008.9:g.61267705C>G	NCBI36
NG_023193.1:g.93804G>C
NG_023193.2:g.93804G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000317995.5:c.*36-2607G>C MANE Select	ENSP00000314407.4:n.*36-2607G>C
ENST00000317995.4:c.*36-2607G>C	ENSP00000314407.4:n.*36-2607G>C
NM_004056.4:c.*36-2607G>C	NP_004047.3:n.*36-2607G>C
XM_011517586.1:c.*36-2607G>C	XP_011515888.1:n.*36-2607G>C
NM_001321839.1:c.*36-2607G>C	NP_001308768.1:n.*36-2607G>C
NM_004056.5:c.*36-2607G>C	NP_004047.3:n.*36-2607G>C
NR_135821.1:n.1235-2607G>C
XM_017013818.1:c.*36-2607G>C	XP_016869307.1:n.*36-2607G>C
NM_004056.6:c.*36-2607G>C MANE Select	NP_004047.3:n.*36-2607G>C
NM_001321839.2:c.*36-2607G>C	NP_001308768.1:n.*36-2607G>C
NR_135821.2:n.1212-2607G>C