Canonical Allele Identifier: CA344876176

Gene: KCNH1

Linked Data

• MyVariant Identifiers: chr1:g.211192422C>G (hg19) ; chr1:g.211019080C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.211019080C>G , CM000663.2:g.211019080C>G	GRCh38
NC_000001.10:g.211192422C>G , CM000663.1:g.211192422C>G	GRCh37
NC_000001.9:g.209259045C>G	NCBI36
NG_029777.1:g.120036G>C
NG_029777.2:g.120036G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271751.10:c.735G>C MANE Select	ENSP00000271751.4:p.Gln245His
ENST00000367007.5:c.735G>C	ENSP00000355974.5:p.Gln245His
ENST00000638357.1:c.149G>C
ENST00000638498.1:c.735G>C	ENSP00000490983.1:p.Gln245His
ENST00000638960.1:c.735G>C	ENSP00000492302.1:p.Gln245His
ENST00000638983.1:c.735G>C	ENSP00000492641.1:p.Gln245His
ENST00000639385.1:n.111G>C
ENST00000639602.1:c.606G>C	ENSP00000492303.1:p.Gln202His
ENST00000639754.1:n.938G>C
ENST00000639952.1:c.735G>C	ENSP00000492697.1:p.Gln245His
ENST00000640044.1:c.310+84416G>C	ENSP00000491434.1:n.310+84416G>C
ENST00000640243.1:c.735G>C	ENSP00000492803.1:p.Gln245His
ENST00000640522.1:c.735G>C	ENSP00000491019.1:p.Gln245His
ENST00000640528.1:c.735G>C	ENSP00000491725.1:p.Gln245His
ENST00000640566.1:c.310+84416G>C	ENSP00000491302.1:n.310+84416G>C
ENST00000640710.1:c.735G>C	ENSP00000492513.1:p.Gln245His
ENST00000640890.1:n.837G>C
ENST00000271751.8:c.735G>C	ENSP00000271751.4:p.Gln245His
ENST00000367007.4:c.735G>C	ENSP00000355974.4:p.Gln245His
NM_002238.3:c.735G>C	NP_002229.1:p.Gln245His
NM_172362.2:c.735G>C	NP_758872.1:p.Gln245His
NM_172362.3:c.735G>C MANE Select	NP_758872.1:p.Gln245His
NM_002238.4:c.735G>C	NP_002229.1:p.Gln245His