Canonical Allele Identifier: CA2830535761

Gene: KCNAB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.156524079_156524080insTTATATTTAGCAGGAGTTTAT , CM000665.2:g.156524079_156524080insTTATATTTAGCAGGAGTTTAT	GRCh38
NC_000003.11:g.156241868_156241869insTTATATTTAGCAGGAGTTTAT , CM000665.1:g.156241868_156241869insTTATATTTAGCAGGAGTTTAT	GRCh37
NC_000003.10:g.157724562_157724563insTTATATTTAGCAGGAGTTTAT	NCBI36
NG_042292.1:g.408532_408533insTTATATTTAGCAGGAGTTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490337.6:c.1081+132_1081+133insTTATATTTAGCAGGAGTTTAT MANE Select	ENSP00000419952.1:n.1081+132_1081+133insTTATATTTAGCAGGAGTTTAT...
ENST00000302490.12:c.1027+132_1027+133insTTATATTTAGCAGGAGTTTAT	ENSP00000305858.8:n.1027+132_1027+133insTTATATTTAGCAGGAGTTTAT...
ENST00000389634.5:c.940+132_940+133insTTATATTTAGCAGGAGTTTAT	ENSP00000374285.5:n.940+132_940+133insTTATATTTAGCAGGAGTTTAT
ENST00000389636.9:c.994+132_994+133insTTATATTTAGCAGGAGTTTAT	ENSP00000374287.5:n.994+132_994+133insTTATATTTAGCAGGAGTTTAT
ENST00000471742.5:c.1048+132_1048+133insTTATATTTAGCAGGAGTTTAT	ENSP00000418956.1:n.1048+132_1048+133insTTATATTTAGCAGGAGTTTAT...
ENST00000490337.5:c.1081+132_1081+133insTTATATTTAGCAGGAGTTTAT	ENSP00000419952.1:n.1081+132_1081+133insTTATATTTAGCAGGAGTTTAT...
ENST00000497291.5:n.873+132_873+133insTTATATTTAGCAGGAGTTTAT
ENST00000618897.4:c.730+132_730+133insTTATATTTAGCAGGAGTTTAT	ENSP00000484368.1:n.730+132_730+133insTTATATTTAGCAGGAGTTTAT
NM_001308217.1:c.994+132_994+133insTTATATTTAGCAGGAGTTTAT	NP_001295146.1:n.994+132_994+133insTTATATTTAGCAGGAGTTTAT
NM_001308222.1:c.940+132_940+133insTTATATTTAGCAGGAGTTTAT	NP_001295151.1:n.940+132_940+133insTTATATTTAGCAGGAGTTTAT
NM_003471.3:c.1048+132_1048+133insTTATATTTAGCAGGAGTTTAT	NP_003462.2:n.1048+132_1048+133insTTATATTTAGCAGGAGTTTAT
NM_172159.3:c.1027+132_1027+133insTTATATTTAGCAGGAGTTTAT	NP_751891.1:n.1027+132_1027+133insTTATATTTAGCAGGAGTTTAT
NM_172160.2:c.1081+132_1081+133insTTATATTTAGCAGGAGTTTAT	NP_751892.1:n.1081+132_1081+133insTTATATTTAGCAGGAGTTTAT
XM_011513115.1:c.835+132_835+133insTTATATTTAGCAGGAGTTTAT	XP_011511417.1:n.835+132_835+133insTTATATTTAGCAGGAGTTTAT
XM_011513116.1:c.826+132_826+133insTTATATTTAGCAGGAGTTTAT	XP_011511418.1:n.826+132_826+133insTTATATTTAGCAGGAGTTTAT
XM_011513117.1:c.709+132_709+133insTTATATTTAGCAGGAGTTTAT	XP_011511419.1:n.709+132_709+133insTTATATTTAGCAGGAGTTTAT
XM_011513115.3:c.835+132_835+133insTTATATTTAGCAGGAGTTTAT	XP_011511417.1:n.835+132_835+133insTTATATTTAGCAGGAGTTTAT
XM_011513116.3:c.826+132_826+133insTTATATTTAGCAGGAGTTTAT	XP_011511418.1:n.826+132_826+133insTTATATTTAGCAGGAGTTTAT
XM_011513117.3:c.709+132_709+133insTTATATTTAGCAGGAGTTTAT	XP_011511419.1:n.709+132_709+133insTTATATTTAGCAGGAGTTTAT
XM_017007171.2:c.835+132_835+133insTTATATTTAGCAGGAGTTTAT	XP_016862660.1:n.835+132_835+133insTTATATTTAGCAGGAGTTTAT
XM_017007173.2:c.709+132_709+133insTTATATTTAGCAGGAGTTTAT	XP_016862662.1:n.709+132_709+133insTTATATTTAGCAGGAGTTTAT
NM_172160.3:c.1081+132_1081+133insTTATATTTAGCAGGAGTTTAT MANE Select	NP_751892.1:n.1081+132_1081+133insTTATATTTAGCAGGAGTTTAT