Canonical Allele Identifier: CA1787831940

Gene: CA8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192814T= , CM000670.2:g.60192814T=	GRCh38
NC_000008.10:g.61105373T= , CM000670.1:g.61105373T=	GRCh37
NC_000008.9:g.61267927T=	NCBI36
NG_023193.1:g.93582A=
NG_023193.2:g.93582A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317995.5:c.*36-2829A= MANE Select	ENSP00000314407.4:n.*36-2829A=
ENST00000317995.4:c.*36-2829A=	ENSP00000314407.4:n.*36-2829A=
NM_004056.4:c.*36-2829A=	NP_004047.3:n.*36-2829A=
XM_011517586.1:c.*36-2829A=	XP_011515888.1:n.*36-2829A=
NM_001321839.1:c.*36-2829A=	NP_001308768.1:n.*36-2829A=
NM_004056.5:c.*36-2829A=	NP_004047.3:n.*36-2829A=
NR_135821.1:n.1235-2829A=
XM_017013818.1:c.*36-2829A=	XP_016869307.1:n.*36-2829A=
NM_004056.6:c.*36-2829A= MANE Select	NP_004047.3:n.*36-2829A=
NM_001321839.2:c.*36-2829A=	NP_001308768.1:n.*36-2829A=
NR_135821.2:n.1212-2829A=