Canonical Allele Identifier: CA369865392

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150671834T>G (hg19) ; chr7:g.150974746T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974746T>G , CM000669.2:g.150974746T>G	GRCh38
NC_000007.13:g.150671834T>G , CM000669.1:g.150671834T>G	GRCh37
NC_000007.12:g.150302767T>G	NCBI36
NG_008916.1:g.8181A>C , LRG_288:g.8181A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262186.10:c.272A>C MANE Select	ENSP00000262186.5:p.Glu91Ala
ENST00000262186.9:c.272A>C	ENSP00000262186.5:p.Glu91Ala
ENST00000430723.4:c.95A>C	ENSP00000387657.4:p.Glu32Ala
ENST00000532957.5:n.495A>C
NM_000238.3:c.272A>C , LRG_288t1:c.272A>C	NP_000229.1:p.Glu91Ala
NM_172056.2:c.272A>C , LRG_288t2:c.272A>C	NP_742053.1:p.Glu91Ala
XM_011516186.1:c.272A>C	XP_011514488.1:p.Glu91Ala
XM_011516186.3:c.272A>C	XP_011514488.1:p.Glu91Ala
XM_017012196.1:c.95A>C	XP_016867685.1:p.Glu32Ala
NM_000238.4:c.272A>C MANE Select	NP_000229.1:p.Glu91Ala