Canonical Allele Identifier: CA1787831713

Gene: CA8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192658_60192659delinsTG , CM000670.2:g.60192658_60192659delinsTG	GRCh38
NC_000008.10:g.61105217_61105218delinsTG , CM000670.1:g.61105217_61105218delinsTG	GRCh37
NC_000008.9:g.61267771_61267772delinsTG	NCBI36
NG_023193.1:g.93737_93738delinsCA
NG_023193.2:g.93737_93738delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000317995.5:c.*36-2674_*36-2673delinsCA MANE Select	ENSP00000314407.4:n.*36-2674_*36-2673deli...
ENST00000317995.4:c.*36-2674_*36-2673delinsCA	ENSP00000314407.4:n.*36-2674_*36-2673deli...
NM_004056.4:c.*36-2674_*36-2673delinsCA	NP_004047.3:n.*36-2674_*36-2673delinsCA
XM_011517586.1:c.*36-2674_*36-2673delinsCA	XP_011515888.1:n.*36-2674_*36-2673delinsC...
NM_001321839.1:c.*36-2674_*36-2673delinsCA	NP_001308768.1:n.*36-2674_*36-2673delinsC...
NM_004056.5:c.*36-2674_*36-2673delinsCA	NP_004047.3:n.*36-2674_*36-2673delinsCA
NR_135821.1:n.1235-2674_1235-2673delinsCA
XM_017013818.1:c.*36-2674_*36-2673delinsCA	XP_016869307.1:n.*36-2674_*36-2673delinsC...
NM_004056.6:c.*36-2674_*36-2673delinsCA MANE Select	NP_004047.3:n.*36-2674_*36-2673delinsCA
NM_001321839.2:c.*36-2674_*36-2673delinsCA	NP_001308768.1:n.*36-2674_*36-2673delinsC...
NR_135821.2:n.1212-2674_1212-2673delinsCA