Canonical Allele Identifier: CA369861632

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150654485A>G (hg19) ; chr7:g.150957397A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957397A>G , CM000669.2:g.150957397A>G	GRCh38
NC_000007.13:g.150654485A>G , CM000669.1:g.150654485A>G	GRCh37
NC_000007.12:g.150285418A>G	NCBI36
NG_008916.1:g.25530T>C , LRG_288:g.25530T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1855T>C
ENST00000262186.10:c.1022T>C MANE Select	ENSP00000262186.5:p.Val341Ala
ENST00000262186.9:c.1022T>C	ENSP00000262186.5:p.Val341Ala
ENST00000430723.4:c.674T>C	ENSP00000387657.4:p.Val225Ala
ENST00000532957.5:n.1245T>C
NM_000238.3:c.1022T>C , LRG_288t1:c.1022T>C	NP_000229.1:p.Val341Ala
NM_172056.2:c.1022T>C , LRG_288t2:c.1022T>C	NP_742053.1:p.Val341Ala
XM_011516185.1:c.722T>C	XP_011514487.1:p.Val241Ala
XM_011516186.1:c.1022T>C	XP_011514488.1:p.Val341Ala
XM_011516185.2:c.722T>C	XP_011514487.1:p.Val241Ala
XM_011516186.3:c.1022T>C	XP_011514488.1:p.Val341Ala
XM_017012195.1:c.872T>C	XP_016867684.1:p.Val291Ala
XM_017012196.1:c.845T>C	XP_016867685.1:p.Val282Ala
NM_000238.4:c.1022T>C MANE Select	NP_000229.1:p.Val341Ala