Canonical Allele Identifier: CA369855278

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150646093G>T (hg19) ; chr7:g.150949005G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150949005G>T , CM000669.2:g.150949005G>T	GRCh38
NC_000007.13:g.150646093G>T , CM000669.1:g.150646093G>T	GRCh37
NC_000007.12:g.150277026G>T	NCBI36
NG_008916.1:g.33922C>A , LRG_288:g.33922C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3276C>A
ENST00000262186.10:c.2443C>A MANE Select	ENSP00000262186.5:p.Pro815Thr
ENST00000330883.9:c.1423C>A	ENSP00000328531.4:p.Pro475Thr
ENST00000262186.9:c.2443C>A	ENSP00000262186.5:p.Pro815Thr
ENST00000330883.8:c.1423C>A	ENSP00000328531.4:p.Pro475Thr
NM_000238.3:c.2443C>A , LRG_288t1:c.2443C>A	NP_000229.1:p.Pro815Thr
NM_172057.2:c.1423C>A , LRG_288t3:c.1423C>A	NP_742054.1:p.Pro475Thr
XM_011516185.1:c.2143C>A	XP_011514487.1:p.Pro715Thr
XM_011516186.1:c.2443C>A	XP_011514488.1:p.Pro815Thr
XM_011516185.2:c.2143C>A	XP_011514487.1:p.Pro715Thr
XM_011516186.3:c.2443C>A	XP_011514488.1:p.Pro815Thr
XM_017012195.1:c.2293C>A	XP_016867684.1:p.Pro765Thr
XM_017012196.1:c.2266C>A	XP_016867685.1:p.Pro756Thr
NM_000238.4:c.2443C>A MANE Select	NP_000229.1:p.Pro815Thr
NM_172057.3:c.1423C>A	NP_742054.1:p.Pro475Thr