Canonical Allele Identifier: CA1752417015
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150957495C= , CM000669.2:g.150957495C= GRCh38
NC_000007.13:g.150654583C= , CM000669.1:g.150654583C= GRCh37
NC_000007.12:g.150285516C= NCBI36
NG_008916.1:g.25432G= , LRG_288:g.25432G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.1757G=
ENST00000262186.10:c.924G= MANE Select ENSP00000262186.5:p.Met308=
ENST00000262186.9:c.924G= ENSP00000262186.5:p.Met308=
ENST00000430723.4:c.576G= ENSP00000387657.4:p.Met192=
ENST00000532957.5:n.1147G=
NM_000238.3:c.924G= , LRG_288t1:c.924G= NP_000229.1:p.Met308=
NM_172056.2:c.924G= , LRG_288t2:c.924G= NP_742053.1:p.Met308=
XM_011516185.1:c.624G= XP_011514487.1:p.Met208=
XM_011516186.1:c.924G= XP_011514488.1:p.Met308=
XM_011516185.2:c.624G= XP_011514487.1:p.Met208=
XM_011516186.3:c.924G= XP_011514488.1:p.Met308=
XM_017012195.1:c.774G= XP_016867684.1:p.Met258=
XM_017012196.1:c.747G= XP_016867685.1:p.Met249=
NM_000238.4:c.924G= MANE Select NP_000229.1:p.Met308=