Canonical Allele Identifier: CA918162841

Gene: KCNH2

Linked Data

• dbSNP Id: rs41313749

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150945527_150945528dup , CM000669.2:g.150945527_150945528dup	GRCh38
NC_000007.13:g.150642615_150642616dup , CM000669.1:g.150642615_150642616dup	GRCh37
NC_000007.12:g.150273548_150273549dup	NCBI36
NG_008916.1:g.37404_37405dup , LRG_288:g.37404_37405dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.4164-9_4164-8dup
ENST00000262186.10:c.3331-9_3331-8dup MANE Select	ENSP00000262186.5:n.3331-9_3331-8dup
ENST00000330883.9:c.2311-9_2311-8dup	ENSP00000328531.4:n.2311-9_2311-8dup
ENST00000262186.9:c.3331-9_3331-8dup	ENSP00000262186.5:n.3331-9_3331-8dup
ENST00000330883.8:c.2311-9_2311-8dup	ENSP00000328531.4:n.2311-9_2311-8dup
NM_000238.3:c.3331-9_3331-8dup , LRG_288t1:c.3331-9_3331-8dup	NP_000229.1:n.3331-9_3331-8dup
NM_172057.2:c.2311-9_2311-8dup , LRG_288t3:c.2311-9_2311-8dup	NP_742054.1:n.2311-9_2311-8dup
XM_011516185.1:c.3031-9_3031-8dup	XP_011514487.1:n.3031-9_3031-8dup
XM_011516185.2:c.3031-9_3031-8dup	XP_011514487.1:n.3031-9_3031-8dup
XM_017012195.1:c.3181-9_3181-8dup	XP_016867684.1:n.3181-9_3181-8dup
XM_017012196.1:c.3154-9_3154-8dup	XP_016867685.1:n.3154-9_3154-8dup
NM_000238.4:c.3331-9_3331-8dup MANE Select	NP_000229.1:n.3331-9_3331-8dup
NM_172057.3:c.2311-9_2311-8dup	NP_742054.1:n.2311-9_2311-8dup