Canonical Allele Identifier: CA2685600457
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948456_150948457dup , CM000669.2:g.150948456_150948457dup GRCh38
NC_000007.13:g.150645544_150645545dup , CM000669.1:g.150645544_150645545dup GRCh37
NC_000007.12:g.150276477_150276478dup NCBI36
NG_008916.1:g.34472_34473dup , LRG_288:g.34472_34473dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.3514_3515dup
ENST00000262186.10:c.2681_2682dup MANE Select ENSP00000262186.5:p.Thr895AlafsTer?
ENST00000330883.9:c.1661_1662dup ENSP00000328531.4:p.Thr555AlafsTer?
ENST00000262186.9:c.2681_2682dup ENSP00000262186.5:p.Thr895AlafsTer?
ENST00000330883.8:c.1661_1662dup ENSP00000328531.4:p.Thr555AlafsTer?
NM_000238.3:c.2681_2682dup , LRG_288t1:c.2681_2682dup NP_000229.1:p.Thr895AlafsTer?
NM_172057.2:c.1661_1662dup , LRG_288t3:c.1661_1662dup NP_742054.1:p.Thr555AlafsTer?
XM_011516185.1:c.2381_2382dup XP_011514487.1:p.Thr795AlafsTer?
XM_011516186.1:c.2681_2682dup XP_011514488.1:p.Thr895AlafsTer?
XM_011516185.2:c.2381_2382dup XP_011514487.1:p.Thr795AlafsTer?
XM_011516186.3:c.2681_2682dup XP_011514488.1:p.Thr895AlafsTer?
XM_017012195.1:c.2531_2532dup XP_016867684.1:p.Thr845AlafsTer?
XM_017012196.1:c.2504_2505dup XP_016867685.1:p.Thr836AlafsTer?
NM_000238.4:c.2681_2682dup MANE Select NP_000229.1:p.Thr895AlafsTer?
NM_172057.3:c.1661_1662dup NP_742054.1:p.Thr555AlafsTer?