Canonical Allele Identifier: CA2717333460

Gene: CA8

Linked Data

• dbSNP Id: rs2130375356

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192509C>A , CM000670.2:g.60192509C>A	GRCh38
NC_000008.10:g.61105068C>A , CM000670.1:g.61105068C>A	GRCh37
NC_000008.9:g.61267622C>A	NCBI36
NG_023193.1:g.93887G>T
NG_023193.2:g.93887G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317995.5:c.*36-2524G>T MANE Select	ENSP00000314407.4:n.*36-2524G>T
ENST00000317995.4:c.*36-2524G>T	ENSP00000314407.4:n.*36-2524G>T
NM_004056.4:c.*36-2524G>T	NP_004047.3:n.*36-2524G>T
XM_011517586.1:c.*36-2524G>T	XP_011515888.1:n.*36-2524G>T
NM_001321839.1:c.*36-2524G>T	NP_001308768.1:n.*36-2524G>T
NM_004056.5:c.*36-2524G>T	NP_004047.3:n.*36-2524G>T
NR_135821.1:n.1235-2524G>T
XM_017013818.1:c.*36-2524G>T	XP_016869307.1:n.*36-2524G>T
NM_004056.6:c.*36-2524G>T MANE Select	NP_004047.3:n.*36-2524G>T
NM_001321839.2:c.*36-2524G>T	NP_001308768.1:n.*36-2524G>T
NR_135821.2:n.1212-2524G>T