Canonical Allele Identifier: CA369857820

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648547A>G (hg19) ; chr7:g.150951459A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951459A>G , CM000669.2:g.150951459A>G	GRCh38
NC_000007.13:g.150648547A>G , CM000669.1:g.150648547A>G	GRCh37
NC_000007.12:g.150279480A>G	NCBI36
NG_008916.1:g.31468T>C , LRG_288:g.31468T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1232T>C
ENST00000683359.1:n.58T>C
ENST00000684241.1:n.2767T>C
ENST00000262186.10:c.1934T>C MANE Select	ENSP00000262186.5:p.Met645Thr
ENST00000330883.9:c.914T>C	ENSP00000328531.4:p.Met305Thr
ENST00000262186.9:c.1934T>C	ENSP00000262186.5:p.Met645Thr
ENST00000330883.8:c.914T>C	ENSP00000328531.4:p.Met305Thr
ENST00000430723.4:c.1586T>C	ENSP00000387657.4:p.Met529Thr
ENST00000461280.1:n.1221T>C
ENST00000473610.5:n.1239T>C
ENST00000532957.5:n.2157T>C
NM_000238.3:c.1934T>C , LRG_288t1:c.1934T>C	NP_000229.1:p.Met645Thr
NM_001204798.1:c.914T>C	NP_001191727.1:p.Met305Thr
NM_172056.2:c.1934T>C , LRG_288t2:c.1934T>C	NP_742053.1:p.Met645Thr
NM_172057.2:c.914T>C , LRG_288t3:c.914T>C	NP_742054.1:p.Met305Thr
XM_011516185.1:c.1634T>C	XP_011514487.1:p.Met545Thr
XM_011516186.1:c.1934T>C	XP_011514488.1:p.Met645Thr
XM_011516185.2:c.1634T>C	XP_011514487.1:p.Met545Thr
XM_011516186.3:c.1934T>C	XP_011514488.1:p.Met645Thr
XM_017012195.1:c.1784T>C	XP_016867684.1:p.Met595Thr
XM_017012196.1:c.1757T>C	XP_016867685.1:p.Met586Thr
NM_000238.4:c.1934T>C MANE Select	NP_000229.1:p.Met645Thr
NM_001204798.2:c.914T>C	NP_001191727.1:p.Met305Thr
NM_172057.3:c.914T>C	NP_742054.1:p.Met305Thr