Canonical Allele Identifier: CA369855282

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150646094C>A (hg19) ; chr7:g.150949006C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150949006C>A , CM000669.2:g.150949006C>A	GRCh38
NC_000007.13:g.150646094C>A , CM000669.1:g.150646094C>A	GRCh37
NC_000007.12:g.150277027C>A	NCBI36
NG_008916.1:g.33921G>T , LRG_288:g.33921G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3275G>T
ENST00000262186.10:c.2442G>T MANE Select	ENSP00000262186.5:p.Arg814Ser
ENST00000330883.9:c.1422G>T	ENSP00000328531.4:p.Arg474Ser
ENST00000262186.9:c.2442G>T	ENSP00000262186.5:p.Arg814Ser
ENST00000330883.8:c.1422G>T	ENSP00000328531.4:p.Arg474Ser
NM_000238.3:c.2442G>T , LRG_288t1:c.2442G>T	NP_000229.1:p.Arg814Ser
NM_172057.2:c.1422G>T , LRG_288t3:c.1422G>T	NP_742054.1:p.Arg474Ser
XM_011516185.1:c.2142G>T	XP_011514487.1:p.Arg714Ser
XM_011516186.1:c.2442G>T	XP_011514488.1:p.Arg814Ser
XM_011516185.2:c.2142G>T	XP_011514487.1:p.Arg714Ser
XM_011516186.3:c.2442G>T	XP_011514488.1:p.Arg814Ser
XM_017012195.1:c.2292G>T	XP_016867684.1:p.Arg764Ser
XM_017012196.1:c.2265G>T	XP_016867685.1:p.Arg755Ser
NM_000238.4:c.2442G>T MANE Select	NP_000229.1:p.Arg814Ser
NM_172057.3:c.1422G>T	NP_742054.1:p.Arg474Ser