Canonical Allele Identifier: CA369853931

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150645622T>G (hg19) ; chr7:g.150948534T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948534T>G , CM000669.2:g.150948534T>G	GRCh38
NC_000007.13:g.150645622T>G , CM000669.1:g.150645622T>G	GRCh37
NC_000007.12:g.150276555T>G	NCBI36
NG_008916.1:g.34393A>C , LRG_288:g.34393A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3435A>C
ENST00000262186.10:c.2602A>C MANE Select	ENSP00000262186.5:p.Ile868Leu
ENST00000330883.9:c.1582A>C	ENSP00000328531.4:p.Ile528Leu
ENST00000262186.9:c.2602A>C	ENSP00000262186.5:p.Ile868Leu
ENST00000330883.8:c.1582A>C	ENSP00000328531.4:p.Ile528Leu
NM_000238.3:c.2602A>C , LRG_288t1:c.2602A>C	NP_000229.1:p.Ile868Leu
NM_172057.2:c.1582A>C , LRG_288t3:c.1582A>C	NP_742054.1:p.Ile528Leu
XM_011516185.1:c.2302A>C	XP_011514487.1:p.Ile768Leu
XM_011516186.1:c.2602A>C	XP_011514488.1:p.Ile868Leu
XM_011516185.2:c.2302A>C	XP_011514487.1:p.Ile768Leu
XM_011516186.3:c.2602A>C	XP_011514488.1:p.Ile868Leu
XM_017012195.1:c.2452A>C	XP_016867684.1:p.Ile818Leu
XM_017012196.1:c.2425A>C	XP_016867685.1:p.Ile809Leu
NM_000238.4:c.2602A>C MANE Select	NP_000229.1:p.Ile868Leu
NM_172057.3:c.1582A>C	NP_742054.1:p.Ile528Leu