Canonical Allele Identifier: CA369854721

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150645960G>C (hg19) ; chr7:g.150948872G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948872G>C , CM000669.2:g.150948872G>C	GRCh38
NC_000007.13:g.150645960G>C , CM000669.1:g.150645960G>C	GRCh37
NC_000007.12:g.150276893G>C	NCBI36
NG_008916.1:g.34055C>G , LRG_288:g.34055C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3409C>G
ENST00000262186.10:c.2576C>G MANE Select	ENSP00000262186.5:p.Thr859Ser
ENST00000330883.9:c.1556C>G	ENSP00000328531.4:p.Thr519Ser
ENST00000262186.9:c.2576C>G	ENSP00000262186.5:p.Thr859Ser
ENST00000330883.8:c.1556C>G	ENSP00000328531.4:p.Thr519Ser
NM_000238.3:c.2576C>G , LRG_288t1:c.2576C>G	NP_000229.1:p.Thr859Ser
NM_172057.2:c.1556C>G , LRG_288t3:c.1556C>G	NP_742054.1:p.Thr519Ser
XM_011516185.1:c.2276C>G	XP_011514487.1:p.Thr759Ser
XM_011516186.1:c.2576C>G	XP_011514488.1:p.Thr859Ser
XM_011516185.2:c.2276C>G	XP_011514487.1:p.Thr759Ser
XM_011516186.3:c.2576C>G	XP_011514488.1:p.Thr859Ser
XM_017012195.1:c.2426C>G	XP_016867684.1:p.Thr809Ser
XM_017012196.1:c.2399C>G	XP_016867685.1:p.Thr800Ser
NM_000238.4:c.2576C>G MANE Select	NP_000229.1:p.Thr859Ser
NM_172057.3:c.1556C>G	NP_742054.1:p.Thr519Ser