Canonical Allele Identifier: CA369854769

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150645972C>G (hg19) ; chr7:g.150948884C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948884C>G , CM000669.2:g.150948884C>G	GRCh38
NC_000007.13:g.150645972C>G , CM000669.1:g.150645972C>G	GRCh37
NC_000007.12:g.150276905C>G	NCBI36
NG_008916.1:g.34043G>C , LRG_288:g.34043G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3397G>C
ENST00000262186.10:c.2564G>C MANE Select	ENSP00000262186.5:p.Ser855Thr
ENST00000330883.9:c.1544G>C	ENSP00000328531.4:p.Ser515Thr
ENST00000262186.9:c.2564G>C	ENSP00000262186.5:p.Ser855Thr
ENST00000330883.8:c.1544G>C	ENSP00000328531.4:p.Ser515Thr
NM_000238.3:c.2564G>C , LRG_288t1:c.2564G>C	NP_000229.1:p.Ser855Thr
NM_172057.2:c.1544G>C , LRG_288t3:c.1544G>C	NP_742054.1:p.Ser515Thr
XM_011516185.1:c.2264G>C	XP_011514487.1:p.Ser755Thr
XM_011516186.1:c.2564G>C	XP_011514488.1:p.Ser855Thr
XM_011516185.2:c.2264G>C	XP_011514487.1:p.Ser755Thr
XM_011516186.3:c.2564G>C	XP_011514488.1:p.Ser855Thr
XM_017012195.1:c.2414G>C	XP_016867684.1:p.Ser805Thr
XM_017012196.1:c.2387G>C	XP_016867685.1:p.Ser796Thr
NM_000238.4:c.2564G>C MANE Select	NP_000229.1:p.Ser855Thr
NM_172057.3:c.1544G>C	NP_742054.1:p.Ser515Thr