Canonical Allele Identifier: CA369853841

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150948513-T-G
• MyVariant Identifiers: chr7:g.150645601T>G (hg19) ; chr7:g.150948513T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948513T>G , CM000669.2:g.150948513T>G	GRCh38
NC_000007.13:g.150645601T>G , CM000669.1:g.150645601T>G	GRCh37
NC_000007.12:g.150276534T>G	NCBI36
NG_008916.1:g.34414A>C , LRG_288:g.34414A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3456A>C
ENST00000262186.10:c.2623A>C MANE Select	ENSP00000262186.5:p.Thr875Pro
ENST00000330883.9:c.1603A>C	ENSP00000328531.4:p.Thr535Pro
ENST00000262186.9:c.2623A>C	ENSP00000262186.5:p.Thr875Pro
ENST00000330883.8:c.1603A>C	ENSP00000328531.4:p.Thr535Pro
NM_000238.3:c.2623A>C , LRG_288t1:c.2623A>C	NP_000229.1:p.Thr875Pro
NM_172057.2:c.1603A>C , LRG_288t3:c.1603A>C	NP_742054.1:p.Thr535Pro
XM_011516185.1:c.2323A>C	XP_011514487.1:p.Thr775Pro
XM_011516186.1:c.2623A>C	XP_011514488.1:p.Thr875Pro
XM_011516185.2:c.2323A>C	XP_011514487.1:p.Thr775Pro
XM_011516186.3:c.2623A>C	XP_011514488.1:p.Thr875Pro
XM_017012195.1:c.2473A>C	XP_016867684.1:p.Thr825Pro
XM_017012196.1:c.2446A>C	XP_016867685.1:p.Thr816Pro
NM_000238.4:c.2623A>C MANE Select	NP_000229.1:p.Thr875Pro
NM_172057.3:c.1603A>C	NP_742054.1:p.Thr535Pro