Canonical Allele Identifier: CA458645926

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150957309-G-A
• MyVariant Identifiers: chr7:g.150654397G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957309G>A , CM000669.2:g.150957309G>A	GRCh38
NC_000007.13:g.150654397G>A , CM000669.1:g.150654397G>A	GRCh37
NC_000007.12:g.150285330G>A	NCBI36
NG_008916.1:g.25618C>T , LRG_288:g.25618C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1943C>T
ENST00000262186.10:c.1110C>T MANE Select	ENSP00000262186.5:p.Val370=
ENST00000262186.9:c.1110C>T	ENSP00000262186.5:p.Val370=
ENST00000430723.4:c.762C>T	ENSP00000387657.4:p.Val254=
ENST00000532957.5:n.1333C>T
NM_000238.3:c.1110C>T , LRG_288t1:c.1110C>T	NP_000229.1:p.Val370=
NM_172056.2:c.1110C>T , LRG_288t2:c.1110C>T	NP_742053.1:p.Val370=
XM_011516185.1:c.810C>T	XP_011514487.1:p.Val270=
XM_011516186.1:c.1110C>T	XP_011514488.1:p.Val370=
XM_011516185.2:c.810C>T	XP_011514487.1:p.Val270=
XM_011516186.3:c.1110C>T	XP_011514488.1:p.Val370=
XM_017012195.1:c.960C>T	XP_016867684.1:p.Val320=
XM_017012196.1:c.933C>T	XP_016867685.1:p.Val311=
NM_000238.4:c.1110C>T MANE Select	NP_000229.1:p.Val370=