Canonical Allele Identifier: CA369862432

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150958173-C-G
• MyVariant Identifiers: chr7:g.150655261C>G (hg19) ; chr7:g.150958173C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958173C>G , CM000669.2:g.150958173C>G	GRCh38
NC_000007.13:g.150655261C>G , CM000669.1:g.150655261C>G	GRCh37
NC_000007.12:g.150286194C>G	NCBI36
NG_008916.1:g.24754G>C , LRG_288:g.24754G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1635G>C
ENST00000262186.10:c.802G>C MANE Select	ENSP00000262186.5:p.Ala268Pro
ENST00000262186.9:c.802G>C	ENSP00000262186.5:p.Ala268Pro
ENST00000430723.4:c.454G>C	ENSP00000387657.4:p.Ala152Pro
ENST00000532957.5:n.1025G>C
NM_000238.3:c.802G>C , LRG_288t1:c.802G>C	NP_000229.1:p.Ala268Pro
NM_172056.2:c.802G>C , LRG_288t2:c.802G>C	NP_742053.1:p.Ala268Pro
XM_011516185.1:c.502G>C	XP_011514487.1:p.Ala168Pro
XM_011516186.1:c.802G>C	XP_011514488.1:p.Ala268Pro
XM_011516185.2:c.502G>C	XP_011514487.1:p.Ala168Pro
XM_011516186.3:c.802G>C	XP_011514488.1:p.Ala268Pro
XM_017012195.1:c.652G>C	XP_016867684.1:p.Ala218Pro
XM_017012196.1:c.625G>C	XP_016867685.1:p.Ala209Pro
NM_000238.4:c.802G>C MANE Select	NP_000229.1:p.Ala268Pro