Canonical Allele Identifier: CA369863846

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150656783T>A (hg19) ; chr7:g.150959695T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959695T>A , CM000669.2:g.150959695T>A	GRCh38
NC_000007.13:g.150656783T>A , CM000669.1:g.150656783T>A	GRCh37
NC_000007.12:g.150287716T>A	NCBI36
NG_008916.1:g.23232A>T , LRG_288:g.23232A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1182A>T
ENST00000262186.10:c.349A>T MANE Select	ENSP00000262186.5:p.Asn117Tyr
ENST00000262186.9:c.349A>T	ENSP00000262186.5:p.Asn117Tyr
ENST00000430723.4:c.172A>T	ENSP00000387657.4:p.Asn58Tyr
ENST00000532957.5:n.572A>T
NM_000238.3:c.349A>T , LRG_288t1:c.349A>T	NP_000229.1:p.Asn117Tyr
NM_172056.2:c.349A>T , LRG_288t2:c.349A>T	NP_742053.1:p.Asn117Tyr
XM_011516185.1:c.49A>T	XP_011514487.1:p.Asn17Tyr
XM_011516186.1:c.349A>T	XP_011514488.1:p.Asn117Tyr
XM_011516185.2:c.49A>T	XP_011514487.1:p.Asn17Tyr
XM_011516186.3:c.349A>T	XP_011514488.1:p.Asn117Tyr
XM_017012195.1:c.199A>T	XP_016867684.1:p.Asn67Tyr
XM_017012196.1:c.172A>T	XP_016867685.1:p.Asn58Tyr
NM_000238.4:c.349A>T MANE Select	NP_000229.1:p.Asn117Tyr