Canonical Allele Identifier: CA369862492

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150655276A>C (hg19) ; chr7:g.150958188A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958188A>C , CM000669.2:g.150958188A>C	GRCh38
NC_000007.13:g.150655276A>C , CM000669.1:g.150655276A>C	GRCh37
NC_000007.12:g.150286209A>C	NCBI36
NG_008916.1:g.24739T>G , LRG_288:g.24739T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1620T>G
ENST00000262186.10:c.787T>G MANE Select	ENSP00000262186.5:p.Ser263Ala
ENST00000262186.9:c.787T>G	ENSP00000262186.5:p.Ser263Ala
ENST00000430723.4:c.439T>G	ENSP00000387657.4:p.Ser147Ala
ENST00000532957.5:n.1010T>G
NM_000238.3:c.787T>G , LRG_288t1:c.787T>G	NP_000229.1:p.Ser263Ala
NM_172056.2:c.787T>G , LRG_288t2:c.787T>G	NP_742053.1:p.Ser263Ala
XM_011516185.1:c.487T>G	XP_011514487.1:p.Ser163Ala
XM_011516186.1:c.787T>G	XP_011514488.1:p.Ser263Ala
XM_011516185.2:c.487T>G	XP_011514487.1:p.Ser163Ala
XM_011516186.3:c.787T>G	XP_011514488.1:p.Ser263Ala
XM_017012195.1:c.637T>G	XP_016867684.1:p.Ser213Ala
XM_017012196.1:c.610T>G	XP_016867685.1:p.Ser204Ala
NM_000238.4:c.787T>G MANE Select	NP_000229.1:p.Ser263Ala