Canonical Allele Identifier: CA369861695

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150654513T>G (hg19) ; chr7:g.150957425T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957425T>G , CM000669.2:g.150957425T>G	GRCh38
NC_000007.13:g.150654513T>G , CM000669.1:g.150654513T>G	GRCh37
NC_000007.12:g.150285446T>G	NCBI36
NG_008916.1:g.25502A>C , LRG_288:g.25502A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1827A>C
ENST00000262186.10:c.994A>C MANE Select	ENSP00000262186.5:p.Lys332Gln
ENST00000262186.9:c.994A>C	ENSP00000262186.5:p.Lys332Gln
ENST00000430723.4:c.646A>C	ENSP00000387657.4:p.Lys216Gln
ENST00000532957.5:n.1217A>C
NM_000238.3:c.994A>C , LRG_288t1:c.994A>C	NP_000229.1:p.Lys332Gln
NM_172056.2:c.994A>C , LRG_288t2:c.994A>C	NP_742053.1:p.Lys332Gln
XM_011516185.1:c.694A>C	XP_011514487.1:p.Lys232Gln
XM_011516186.1:c.994A>C	XP_011514488.1:p.Lys332Gln
XM_011516185.2:c.694A>C	XP_011514487.1:p.Lys232Gln
XM_011516186.3:c.994A>C	XP_011514488.1:p.Lys332Gln
XM_017012195.1:c.844A>C	XP_016867684.1:p.Lys282Gln
XM_017012196.1:c.817A>C	XP_016867685.1:p.Lys273Gln
NM_000238.4:c.994A>C MANE Select	NP_000229.1:p.Lys332Gln