Canonical Allele Identifier: CA1752446554
Gene: KCNH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150977917G= , CM000669.2:g.150977917G= GRCh38
NC_000007.13:g.150675005G= , CM000669.1:g.150675005G= GRCh37
NC_000007.12:g.150305938G= NCBI36
NG_008916.1:g.5010C= , LRG_288:g.5010C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262186.10:c.-4C= MANE Select ENSP00000262186.5:n.-4C=
ENST00000262186.9:c.-4C= ENSP00000262186.5:n.-4C=
ENST00000430723.4:c.-181C= ENSP00000387657.4:n.-181C=
ENST00000532957.5:n.220C=
NM_000238.3:c.-4C= , LRG_288t1:c.-4C= NP_000229.1:n.-4C=
NM_172056.2:c.-4C= , LRG_288t2:c.-4C= NP_742053.1:n.-4C=
XM_011516186.1:c.-4C= XP_011514488.1:n.-4C=
XM_011516186.3:c.-4C= XP_011514488.1:n.-4C=
NM_000238.4:c.-4C= MANE Select NP_000229.1:n.-4C=
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