Canonical Allele Identifier: CA369851624

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150642598G>T (hg19) ; chr7:g.150945510G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150945510G>T , CM000669.2:g.150945510G>T	GRCh38
NC_000007.13:g.150642598G>T , CM000669.1:g.150642598G>T	GRCh37
NC_000007.12:g.150273531G>T	NCBI36
NG_008916.1:g.37417C>A , LRG_288:g.37417C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.4168C>A
ENST00000262186.10:c.3335C>A MANE Select	ENSP00000262186.5:p.Ser1112Tyr
ENST00000330883.9:c.2315C>A	ENSP00000328531.4:p.Ser772Tyr
ENST00000262186.9:c.3335C>A	ENSP00000262186.5:p.Ser1112Tyr
ENST00000330883.8:c.2315C>A	ENSP00000328531.4:p.Ser772Tyr
NM_000238.3:c.3335C>A , LRG_288t1:c.3335C>A	NP_000229.1:p.Ser1112Tyr
NM_172057.2:c.2315C>A , LRG_288t3:c.2315C>A	NP_742054.1:p.Ser772Tyr
XM_011516185.1:c.3035C>A	XP_011514487.1:p.Ser1012Tyr
XM_011516185.2:c.3035C>A	XP_011514487.1:p.Ser1012Tyr
XM_017012195.1:c.3185C>A	XP_016867684.1:p.Ser1062Tyr
XM_017012196.1:c.3158C>A	XP_016867685.1:p.Ser1053Tyr
NM_000238.4:c.3335C>A MANE Select	NP_000229.1:p.Ser1112Tyr
NM_172057.3:c.2315C>A	NP_742054.1:p.Ser772Tyr