Canonical Allele Identifier: CA1787831901

Gene: CA8

Linked Data

• dbSNP Id: rs1806166859

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192791_60192792insAAGTC , CM000670.2:g.60192791_60192792insAAGTC	GRCh38
NC_000008.10:g.61105350_61105351insAAGTC , CM000670.1:g.61105350_61105351insAAGTC	GRCh37
NC_000008.9:g.61267904_61267905insAAGTC	NCBI36
NG_023193.1:g.93606_93607insCTTGA
NG_023193.2:g.93606_93607insCTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317995.5:c.*36-2805_*36-2804insCTTGA MANE Select	ENSP00000314407.4:n.*36-2805_*36-2804insCTTGA
ENST00000317995.4:c.*36-2805_*36-2804insCTTGA	ENSP00000314407.4:n.*36-2805_*36-2804insCTTGA
NM_004056.4:c.*36-2805_*36-2804insCTTGA	NP_004047.3:n.*36-2805_*36-2804insCTTGA
XM_011517586.1:c.*36-2805_*36-2804insCTTGA	XP_011515888.1:n.*36-2805_*36-2804insCTTGA
NM_001321839.1:c.*36-2805_*36-2804insCTTGA	NP_001308768.1:n.*36-2805_*36-2804insCTTGA
NM_004056.5:c.*36-2805_*36-2804insCTTGA	NP_004047.3:n.*36-2805_*36-2804insCTTGA
NR_135821.1:n.1235-2805_1235-2804insCTTGA
XM_017013818.1:c.*36-2805_*36-2804insCTTGA	XP_016869307.1:n.*36-2805_*36-2804insCTTGA
NM_004056.6:c.*36-2805_*36-2804insCTTGA MANE Select	NP_004047.3:n.*36-2805_*36-2804insCTTGA
NM_001321839.2:c.*36-2805_*36-2804insCTTGA	NP_001308768.1:n.*36-2805_*36-2804insCTTGA
NR_135821.2:n.1212-2805_1212-2804insCTTGA