Canonical Allele Identifier: CA369852528

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150947346-A-G
• MyVariant Identifiers: chr7:g.150644434A>G (hg19) ; chr7:g.150947346A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947346A>G , CM000669.2:g.150947346A>G	GRCh38
NC_000007.13:g.150644434A>G , CM000669.1:g.150644434A>G	GRCh37
NC_000007.12:g.150275367A>G	NCBI36
NG_008916.1:g.35581T>C , LRG_288:g.35581T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3967T>C
ENST00000262186.10:c.3134T>C MANE Select	ENSP00000262186.5:p.Leu1045Pro
ENST00000330883.9:c.2114T>C	ENSP00000328531.4:p.Leu705Pro
ENST00000262186.9:c.3134T>C	ENSP00000262186.5:p.Leu1045Pro
ENST00000330883.8:c.2114T>C	ENSP00000328531.4:p.Leu705Pro
NM_000238.3:c.3134T>C , LRG_288t1:c.3134T>C	NP_000229.1:p.Leu1045Pro
NM_172057.2:c.2114T>C , LRG_288t3:c.2114T>C	NP_742054.1:p.Leu705Pro
XM_011516185.1:c.2834T>C	XP_011514487.1:p.Leu945Pro
XM_011516185.2:c.2834T>C	XP_011514487.1:p.Leu945Pro
XM_017012195.1:c.2984T>C	XP_016867684.1:p.Leu995Pro
XM_017012196.1:c.2957T>C	XP_016867685.1:p.Leu986Pro
NM_000238.4:c.3134T>C MANE Select	NP_000229.1:p.Leu1045Pro
NM_172057.3:c.2114T>C	NP_742054.1:p.Leu705Pro