Canonical Allele Identifier: CA369863831

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150656776T>G (hg19) ; chr7:g.150959688T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959688T>G , CM000669.2:g.150959688T>G	GRCh38
NC_000007.13:g.150656776T>G , CM000669.1:g.150656776T>G	GRCh37
NC_000007.12:g.150287709T>G	NCBI36
NG_008916.1:g.23239A>C , LRG_288:g.23239A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1189A>C
ENST00000262186.10:c.356A>C MANE Select	ENSP00000262186.5:p.Asp119Ala
ENST00000262186.9:c.356A>C	ENSP00000262186.5:p.Asp119Ala
ENST00000430723.4:c.179A>C	ENSP00000387657.4:p.Asp60Ala
ENST00000532957.5:n.579A>C
NM_000238.3:c.356A>C , LRG_288t1:c.356A>C	NP_000229.1:p.Asp119Ala
NM_172056.2:c.356A>C , LRG_288t2:c.356A>C	NP_742053.1:p.Asp119Ala
XM_011516185.1:c.56A>C	XP_011514487.1:p.Asp19Ala
XM_011516186.1:c.356A>C	XP_011514488.1:p.Asp119Ala
XM_011516185.2:c.56A>C	XP_011514487.1:p.Asp19Ala
XM_011516186.3:c.356A>C	XP_011514488.1:p.Asp119Ala
XM_017012195.1:c.206A>C	XP_016867684.1:p.Asp69Ala
XM_017012196.1:c.179A>C	XP_016867685.1:p.Asp60Ala
NM_000238.4:c.356A>C MANE Select	NP_000229.1:p.Asp119Ala