Canonical Allele Identifier: CA369854724

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150645961T>A (hg19) ; chr7:g.150948873T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948873T>A , CM000669.2:g.150948873T>A	GRCh38
NC_000007.13:g.150645961T>A , CM000669.1:g.150645961T>A	GRCh37
NC_000007.12:g.150276894T>A	NCBI36
NG_008916.1:g.34054A>T , LRG_288:g.34054A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3408A>T
ENST00000262186.10:c.2575A>T MANE Select	ENSP00000262186.5:p.Thr859Ser
ENST00000330883.9:c.1555A>T	ENSP00000328531.4:p.Thr519Ser
ENST00000262186.9:c.2575A>T	ENSP00000262186.5:p.Thr859Ser
ENST00000330883.8:c.1555A>T	ENSP00000328531.4:p.Thr519Ser
NM_000238.3:c.2575A>T , LRG_288t1:c.2575A>T	NP_000229.1:p.Thr859Ser
NM_172057.2:c.1555A>T , LRG_288t3:c.1555A>T	NP_742054.1:p.Thr519Ser
XM_011516185.1:c.2275A>T	XP_011514487.1:p.Thr759Ser
XM_011516186.1:c.2575A>T	XP_011514488.1:p.Thr859Ser
XM_011516185.2:c.2275A>T	XP_011514487.1:p.Thr759Ser
XM_011516186.3:c.2575A>T	XP_011514488.1:p.Thr859Ser
XM_017012195.1:c.2425A>T	XP_016867684.1:p.Thr809Ser
XM_017012196.1:c.2398A>T	XP_016867685.1:p.Thr800Ser
NM_000238.4:c.2575A>T MANE Select	NP_000229.1:p.Thr859Ser
NM_172057.3:c.1555A>T	NP_742054.1:p.Thr519Ser