Canonical Allele Identifier: CA1413357594

Gene: KCNAB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.156384945C= , CM000665.2:g.156384945C=	GRCh38
NC_000003.11:g.156102734C= , CM000665.1:g.156102734C=	GRCh37
NC_000003.10:g.157585428C=	NCBI36
NG_042292.1:g.269398C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490337.6:c.276-36671C= MANE Select	ENSP00000419952.1:n.276-36671C=
ENST00000302490.12:c.222-36671C=	ENSP00000305858.8:n.222-36671C=
ENST00000389634.5:c.222-36671C=	ENSP00000374285.5:n.222-36671C=
ENST00000389636.9:c.276-36671C=	ENSP00000374287.5:n.276-36671C=
ENST00000471742.5:c.243-36671C=	ENSP00000418956.1:n.243-36671C=
ENST00000472028.5:c.30-36671C=	ENSP00000420755.1:n.30-36671C=
ENST00000475456.5:c.105-36671C=	ENSP00000420221.1:n.105-36671C=
ENST00000477912.5:n.241+2737C=
ENST00000478609.5:n.175-36671C=
ENST00000489036.5:c.210-67954C=	ENSP00000418048.1:n.210-67954C=
ENST00000490337.5:c.276-36671C=	ENSP00000419952.1:n.276-36671C=
ENST00000618897.4:c.12-36671C=	ENSP00000484368.1:n.12-36671C=
NM_001308217.1:c.276-36671C=	NP_001295146.1:n.276-36671C=
NM_001308222.1:c.222-36671C=	NP_001295151.1:n.222-36671C=
NM_003471.3:c.243-36671C=	NP_003462.2:n.243-36671C=
NM_172159.3:c.222-36671C=	NP_751891.1:n.222-36671C=
NM_172160.2:c.276-36671C=	NP_751892.1:n.276-36671C=
XM_011513115.1:c.30-36671C=	XP_011511417.1:n.30-36671C=
XM_011513115.3:c.30-36671C=	XP_011511417.1:n.30-36671C=
XM_017007171.2:c.30-36671C=	XP_016862660.1:n.30-36671C=
XM_017007174.2:c.276-36671C=	XP_016862663.1:n.276-36671C=
NM_172160.3:c.276-36671C= MANE Select	NP_751892.1:n.276-36671C=