Canonical Allele Identifier: CA369852796

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150644513T>A (hg19) ; chr7:g.150947425T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947425T>A , CM000669.2:g.150947425T>A	GRCh38
NC_000007.13:g.150644513T>A , CM000669.1:g.150644513T>A	GRCh37
NC_000007.12:g.150275446T>A	NCBI36
NG_008916.1:g.35502A>T , LRG_288:g.35502A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3888A>T
ENST00000262186.10:c.3055A>T MANE Select	ENSP00000262186.5:p.Thr1019Ser
ENST00000330883.9:c.2035A>T	ENSP00000328531.4:p.Thr679Ser
ENST00000262186.9:c.3055A>T	ENSP00000262186.5:p.Thr1019Ser
ENST00000330883.8:c.2035A>T	ENSP00000328531.4:p.Thr679Ser
NM_000238.3:c.3055A>T , LRG_288t1:c.3055A>T	NP_000229.1:p.Thr1019Ser
NM_172057.2:c.2035A>T , LRG_288t3:c.2035A>T	NP_742054.1:p.Thr679Ser
XM_011516185.1:c.2755A>T	XP_011514487.1:p.Thr919Ser
XM_011516186.1:c.*135A>T	XP_011514488.1:n.*135A>T
XM_011516185.2:c.2755A>T	XP_011514487.1:p.Thr919Ser
XM_011516186.3:c.*135A>T	XP_011514488.1:n.*135A>T
XM_017012195.1:c.2905A>T	XP_016867684.1:p.Thr969Ser
XM_017012196.1:c.2878A>T	XP_016867685.1:p.Thr960Ser
NM_000238.4:c.3055A>T MANE Select	NP_000229.1:p.Thr1019Ser
NM_172057.3:c.2035A>T	NP_742054.1:p.Thr679Ser