Canonical Allele Identifier: CA272069277

Gene: CA12

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.63327516dup , CM000677.2:g.63327516dup	GRCh38
NC_000015.9:g.63619715dup , CM000677.1:g.63619715dup	GRCh37
NC_000015.8:g.61406768dup	NCBI36
NG_028022.1:g.59376dup
NG_028022.2:g.59666dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001218.5:c.908-268dup MANE Select	NP_001209.1:n.908-268dup
ENST00000178638.8:c.908-268dup MANE Select	ENSP00000178638.3:n.908-268dup
NM_001218.4:c.908-268dup	NP_001209.1:n.908-268dup
NM_001293642.1:c.695-268dup	NP_001280571.1:n.695-268dup
NM_001293642.2:c.695-268dup	NP_001280571.1:n.695-268dup
NM_206925.2:c.875-268dup	NP_996808.1:n.875-268dup
NM_206925.3:c.875-268dup	NP_996808.1:n.875-268dup
NR_135511.1:n.1368-268dup
NR_135511.2:n.1048-268dup
ENST00000178638.7:c.908-268dup	ENSP00000178638.3:n.908-268dup
ENST00000344366.7:c.875-268dup	ENSP00000343088.3:n.875-268dup
ENST00000422263.2:c.695-268dup	ENSP00000403028.2:n.695-268dup
ENST00000560666.1:n.118-268dup
XR_932358.1:n.767+8762dup