Canonical Allele Identifier: CA369863604

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150656668A>T (hg19) ; chr7:g.150959580A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959580A>T , CM000669.2:g.150959580A>T	GRCh38
NC_000007.13:g.150656668A>T , CM000669.1:g.150656668A>T	GRCh37
NC_000007.12:g.150287601A>T	NCBI36
NG_008916.1:g.23347T>A , LRG_288:g.23347T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1297T>A
ENST00000262186.10:c.464T>A MANE Select	ENSP00000262186.5:p.Leu155Gln
ENST00000262186.9:c.464T>A	ENSP00000262186.5:p.Leu155Gln
ENST00000430723.4:c.234+53T>A	ENSP00000387657.4:n.234+53T>A
ENST00000532957.5:n.687T>A
NM_000238.3:c.464T>A , LRG_288t1:c.464T>A	NP_000229.1:p.Leu155Gln
NM_172056.2:c.464T>A , LRG_288t2:c.464T>A	NP_742053.1:p.Leu155Gln
XM_011516185.1:c.164T>A	XP_011514487.1:p.Leu55Gln
XM_011516186.1:c.464T>A	XP_011514488.1:p.Leu155Gln
XM_011516185.2:c.164T>A	XP_011514487.1:p.Leu55Gln
XM_011516186.3:c.464T>A	XP_011514488.1:p.Leu155Gln
XM_017012195.1:c.314T>A	XP_016867684.1:p.Leu105Gln
XM_017012196.1:c.287T>A	XP_016867685.1:p.Leu96Gln
NM_000238.4:c.464T>A MANE Select	NP_000229.1:p.Leu155Gln