Canonical Allele Identifier: CA12726843

Gene: CA8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60281284C>G , CM000670.2:g.60281284C>G	GRCh38
NC_000008.10:g.61193843C>G , CM000670.1:g.61193843C>G	GRCh37
NC_000008.9:g.61356397C>G	NCBI36
NG_023193.1:g.5112G>C
NG_023193.2:g.5112G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004056.6:c.-137G>C MANE Select	NP_004047.3:n.-137G>C
ENST00000317995.5:c.-137G>C MANE Select	ENSP00000314407.4:n.-137G>C
NM_001321837.1:c.-137G>C	NP_001308766.1:n.-137G>C
NM_001321837.2:c.-137G>C	NP_001308766.1:n.-137G>C
NM_001321838.1:c.-137G>C	NP_001308767.1:n.-137G>C
NM_001321838.2:c.-137G>C	NP_001308767.1:n.-137G>C
NM_001321839.1:c.-137G>C	NP_001308768.1:n.-137G>C
NM_001321839.2:c.-137G>C	NP_001308768.1:n.-137G>C
NM_004056.4:c.-137G>C	NP_004047.3:n.-137G>C
NM_004056.5:c.-137G>C	NP_004047.3:n.-137G>C
NR_135821.1:n.140G>C
NR_135821.2:n.117G>C
ENST00000317995.4:c.-137G>C	ENSP00000314407.4:n.-137G>C
ENST00000524872.5:n.102G>C
ENST00000529918.1:n.41G>C
XM_011517585.1:c.-137G>C	XP_011515887.1:n.-137G>C
XM_011517586.1:c.-137G>C	XP_011515888.1:n.-137G>C
XM_011517587.1:c.-137G>C	XP_011515889.1:n.-137G>C
XM_011517587.2:c.-137G>C	XP_011515889.1:n.-137G>C
XM_011517588.1:c.-137G>C	XP_011515890.1:n.-137G>C
XM_011517588.3:c.-137G>C	XP_011515890.1:n.-137G>C
XM_017013818.1:c.-482G>C	XP_016869307.1:n.-482G>C