Canonical Allele Identifier: CA369855375

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150646125A>C (hg19) ; chr7:g.150949037A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150949037A>C , CM000669.2:g.150949037A>C	GRCh38
NC_000007.13:g.150646125A>C , CM000669.1:g.150646125A>C	GRCh37
NC_000007.12:g.150277058A>C	NCBI36
NG_008916.1:g.33890T>G , LRG_288:g.33890T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3244T>G
ENST00000262186.10:c.2411T>G MANE Select	ENSP00000262186.5:p.Ile804Ser
ENST00000330883.9:c.1391T>G	ENSP00000328531.4:p.Ile464Ser
ENST00000262186.9:c.2411T>G	ENSP00000262186.5:p.Ile804Ser
ENST00000330883.8:c.1391T>G	ENSP00000328531.4:p.Ile464Ser
NM_000238.3:c.2411T>G , LRG_288t1:c.2411T>G	NP_000229.1:p.Ile804Ser
NM_172057.2:c.1391T>G , LRG_288t3:c.1391T>G	NP_742054.1:p.Ile464Ser
XM_011516185.1:c.2111T>G	XP_011514487.1:p.Ile704Ser
XM_011516186.1:c.2411T>G	XP_011514488.1:p.Ile804Ser
XM_011516185.2:c.2111T>G	XP_011514487.1:p.Ile704Ser
XM_011516186.3:c.2411T>G	XP_011514488.1:p.Ile804Ser
XM_017012195.1:c.2261T>G	XP_016867684.1:p.Ile754Ser
XM_017012196.1:c.2234T>G	XP_016867685.1:p.Ile745Ser
NM_000238.4:c.2411T>G MANE Select	NP_000229.1:p.Ile804Ser
NM_172057.3:c.1391T>G	NP_742054.1:p.Ile464Ser