Canonical Allele Identifier: CA369862273

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150958125-A-C
• MyVariant Identifiers: chr7:g.150655213A>C (hg19) ; chr7:g.150958125A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958125A>C , CM000669.2:g.150958125A>C	GRCh38
NC_000007.13:g.150655213A>C , CM000669.1:g.150655213A>C	GRCh37
NC_000007.12:g.150286146A>C	NCBI36
NG_008916.1:g.24802T>G , LRG_288:g.24802T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1683T>G
ENST00000262186.10:c.850T>G MANE Select	ENSP00000262186.5:p.Ser284Ala
ENST00000262186.9:c.850T>G	ENSP00000262186.5:p.Ser284Ala
ENST00000430723.4:c.502T>G	ENSP00000387657.4:p.Ser168Ala
ENST00000532957.5:n.1073T>G
NM_000238.3:c.850T>G , LRG_288t1:c.850T>G	NP_000229.1:p.Ser284Ala
NM_172056.2:c.850T>G , LRG_288t2:c.850T>G	NP_742053.1:p.Ser284Ala
XM_011516185.1:c.550T>G	XP_011514487.1:p.Ser184Ala
XM_011516186.1:c.850T>G	XP_011514488.1:p.Ser284Ala
XM_011516185.2:c.550T>G	XP_011514487.1:p.Ser184Ala
XM_011516186.3:c.850T>G	XP_011514488.1:p.Ser284Ala
XM_017012195.1:c.700T>G	XP_016867684.1:p.Ser234Ala
XM_017012196.1:c.673T>G	XP_016867685.1:p.Ser225Ala
NM_000238.4:c.850T>G MANE Select	NP_000229.1:p.Ser284Ala