Canonical Allele Identifier: CA369853489

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150947834-C-A
• COSMIC: COSM6401645 ; COSM6401646
• MyVariant Identifiers: chr7:g.150644922C>A (hg19) ; chr7:g.150947834C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947834C>A , CM000669.2:g.150947834C>A	GRCh38
NC_000007.13:g.150644922C>A , CM000669.1:g.150644922C>A	GRCh37
NC_000007.12:g.150275855C>A	NCBI36
NG_008916.1:g.35093G>T , LRG_288:g.35093G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3570G>T
ENST00000262186.10:c.2737G>T MANE Select	ENSP00000262186.5:p.Ala913Ser
ENST00000330883.9:c.1717G>T	ENSP00000328531.4:p.Ala573Ser
ENST00000262186.9:c.2737G>T	ENSP00000262186.5:p.Ala913Ser
ENST00000330883.8:c.1717G>T	ENSP00000328531.4:p.Ala573Ser
NM_000238.3:c.2737G>T , LRG_288t1:c.2737G>T	NP_000229.1:p.Ala913Ser
NM_172057.2:c.1717G>T , LRG_288t3:c.1717G>T	NP_742054.1:p.Ala573Ser
XM_011516185.1:c.2437G>T	XP_011514487.1:p.Ala813Ser
XM_011516186.1:c.2693-143G>T	XP_011514488.1:n.2693-143G>T
XM_011516185.2:c.2437G>T	XP_011514487.1:p.Ala813Ser
XM_011516186.3:c.2693-143G>T	XP_011514488.1:n.2693-143G>T
XM_017012195.1:c.2587G>T	XP_016867684.1:p.Ala863Ser
XM_017012196.1:c.2560G>T	XP_016867685.1:p.Ala854Ser
NM_000238.4:c.2737G>T MANE Select	NP_000229.1:p.Ala913Ser
NM_172057.3:c.1717G>T	NP_742054.1:p.Ala573Ser