Canonical Allele Identifier: CA344873569

Gene: KCNH1

Linked Data

• gnomAD v4: 1-210919890-C-A
• MyVariant Identifiers: chr1:g.211093232C>A (hg19) ; chr1:g.210919890C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.210919890C>A , CM000663.2:g.210919890C>A	GRCh38
NC_000001.10:g.211093232C>A , CM000663.1:g.211093232C>A	GRCh37
NC_000001.9:g.209159855C>A	NCBI36
NG_029777.1:g.219226G>T
NG_029777.2:g.219226G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000271751.10:c.1212G>T MANE Select	ENSP00000271751.4:p.Glu404Asp
ENST00000367007.5:c.1131G>T	ENSP00000355974.5:p.Glu377Asp
ENST00000638357.1:c.545G>T
ENST00000638498.1:c.1212G>T	ENSP00000490983.1:p.Glu404Asp
ENST00000638960.1:c.1131G>T	ENSP00000492302.1:p.Glu377Asp
ENST00000638983.1:c.952-58696G>T	ENSP00000492641.1:n.952-58696G>T
ENST00000639385.1:n.580G>T
ENST00000639602.1:c.1002G>T	ENSP00000492303.1:p.Glu334Asp
ENST00000639754.1:n.1415G>T
ENST00000639952.1:c.1131G>T	ENSP00000492697.1:p.Glu377Asp
ENST00000640044.1:c.311-115724G>T	ENSP00000491434.1:n.311-115724G>T
ENST00000640243.1:c.951+98974G>T	ENSP00000492803.1:n.951+98974G>T
ENST00000640522.1:c.1032+98893G>T	ENSP00000491019.1:n.1032+98893G>T
ENST00000640528.1:c.1131G>T	ENSP00000491725.1:p.Glu377Asp
ENST00000640566.1:c.311-144346G>T	ENSP00000491302.1:n.311-144346G>T
ENST00000640710.1:c.1131G>T	ENSP00000492513.1:p.Glu377Asp
ENST00000640890.1:n.1233G>T
ENST00000271751.8:c.1212G>T	ENSP00000271751.4:p.Glu404Asp
ENST00000367007.4:c.1131G>T	ENSP00000355974.4:p.Glu377Asp
NM_002238.3:c.1131G>T	NP_002229.1:p.Glu377Asp
NM_172362.2:c.1212G>T	NP_758872.1:p.Glu404Asp
XM_011509514.1:c.36G>T	XP_011507816.1:p.Glu12Asp
XM_017001246.1:c.36G>T	XP_016856735.1:p.Glu12Asp
NM_172362.3:c.1212G>T MANE Select	NP_758872.1:p.Glu404Asp
NM_002238.4:c.1131G>T	NP_002229.1:p.Glu377Asp