Canonical Allele Identifier: CA178119072

Gene: CA8

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192458A>T , CM000670.2:g.60192458A>T	GRCh38
NC_000008.10:g.61105017A>T , CM000670.1:g.61105017A>T	GRCh37
NC_000008.9:g.61267571A>T	NCBI36
NG_023193.1:g.93938T>A
NG_023193.2:g.93938T>A

Transcript Alleles

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