Canonical Allele Identifier: CA369855198

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150646075C>G (hg19) ; chr7:g.150948987C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948987C>G , CM000669.2:g.150948987C>G	GRCh38
NC_000007.13:g.150646075C>G , CM000669.1:g.150646075C>G	GRCh37
NC_000007.12:g.150277008C>G	NCBI36
NG_008916.1:g.33940G>C , LRG_288:g.33940G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3294G>C
ENST00000262186.10:c.2461G>C MANE Select	ENSP00000262186.5:p.Asp821His
ENST00000330883.9:c.1441G>C	ENSP00000328531.4:p.Asp481His
ENST00000262186.9:c.2461G>C	ENSP00000262186.5:p.Asp821His
ENST00000330883.8:c.1441G>C	ENSP00000328531.4:p.Asp481His
NM_000238.3:c.2461G>C , LRG_288t1:c.2461G>C	NP_000229.1:p.Asp821His
NM_172057.2:c.1441G>C , LRG_288t3:c.1441G>C	NP_742054.1:p.Asp481His
XM_011516185.1:c.2161G>C	XP_011514487.1:p.Asp721His
XM_011516186.1:c.2461G>C	XP_011514488.1:p.Asp821His
XM_011516185.2:c.2161G>C	XP_011514487.1:p.Asp721His
XM_011516186.3:c.2461G>C	XP_011514488.1:p.Asp821His
XM_017012195.1:c.2311G>C	XP_016867684.1:p.Asp771His
XM_017012196.1:c.2284G>C	XP_016867685.1:p.Asp762His
NM_000238.4:c.2461G>C MANE Select	NP_000229.1:p.Asp821His
NM_172057.3:c.1441G>C	NP_742054.1:p.Asp481His