Canonical Allele Identifier: CA1752409431
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951489T= , CM000669.2:g.150951489T= GRCh38
NC_000007.13:g.150648577T= , CM000669.1:g.150648577T= GRCh37
NC_000007.12:g.150279510T= NCBI36
NG_008916.1:g.31438A= , LRG_288:g.31438A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1202A=
ENST00000683359.1:n.28A=
ENST00000684241.1:n.2737A=
ENST00000262186.10:c.1904A= MANE Select ENSP00000262186.5:p.Asn635=
ENST00000330883.9:c.884A= ENSP00000328531.4:p.Asn295=
ENST00000262186.9:c.1904A= ENSP00000262186.5:p.Asn635=
ENST00000330883.8:c.884A= ENSP00000328531.4:p.Asn295=
ENST00000430723.4:c.1556A= ENSP00000387657.4:p.Asn519=
ENST00000461280.1:n.1191A=
ENST00000473610.5:n.1209A=
ENST00000532957.5:n.2127A=
NM_000238.3:c.1904A= , LRG_288t1:c.1904A= NP_000229.1:p.Asn635=
NM_001204798.1:c.884A= NP_001191727.1:p.Asn295=
NM_172056.2:c.1904A= , LRG_288t2:c.1904A= NP_742053.1:p.Asn635=
NM_172057.2:c.884A= , LRG_288t3:c.884A= NP_742054.1:p.Asn295=
XM_011516185.1:c.1604A= XP_011514487.1:p.Asn535=
XM_011516186.1:c.1904A= XP_011514488.1:p.Asn635=
XM_011516185.2:c.1604A= XP_011514487.1:p.Asn535=
XM_011516186.3:c.1904A= XP_011514488.1:p.Asn635=
XM_017012195.1:c.1754A= XP_016867684.1:p.Asn585=
XM_017012196.1:c.1727A= XP_016867685.1:p.Asn576=
NM_000238.4:c.1904A= MANE Select NP_000229.1:p.Asn635=
NM_001204798.2:c.884A= NP_001191727.1:p.Asn295=
NM_172057.3:c.884A= NP_742054.1:p.Asn295=