Canonical Allele Identifier: CA369851620

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150642595T>G (hg19) ; chr7:g.150945507T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150945507T>G , CM000669.2:g.150945507T>G	GRCh38
NC_000007.13:g.150642595T>G , CM000669.1:g.150642595T>G	GRCh37
NC_000007.12:g.150273528T>G	NCBI36
NG_008916.1:g.37420A>C , LRG_288:g.37420A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.4171A>C
ENST00000262186.10:c.3338A>C MANE Select	ENSP00000262186.5:p.Gln1113Pro
ENST00000330883.9:c.2318A>C	ENSP00000328531.4:p.Gln773Pro
ENST00000262186.9:c.3338A>C	ENSP00000262186.5:p.Gln1113Pro
ENST00000330883.8:c.2318A>C	ENSP00000328531.4:p.Gln773Pro
NM_000238.3:c.3338A>C , LRG_288t1:c.3338A>C	NP_000229.1:p.Gln1113Pro
NM_172057.2:c.2318A>C , LRG_288t3:c.2318A>C	NP_742054.1:p.Gln773Pro
XM_011516185.1:c.3038A>C	XP_011514487.1:p.Gln1013Pro
XM_011516185.2:c.3038A>C	XP_011514487.1:p.Gln1013Pro
XM_017012195.1:c.3188A>C	XP_016867684.1:p.Gln1063Pro
XM_017012196.1:c.3161A>C	XP_016867685.1:p.Gln1054Pro
NM_000238.4:c.3338A>C MANE Select	NP_000229.1:p.Gln1113Pro
NM_172057.3:c.2318A>C	NP_742054.1:p.Gln773Pro