Canonical Allele Identifier: CA730899994

Gene: KCNH1

Linked Data

• dbSNP Id: rs1260646098
• gnomAD v3: 1-210804352-A-G
• gnomAD v4: 1-210804352-A-G
• MyVariant Identifiers: chr1:g.210977694A>G (hg19) ; chr1:g.210804352A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.210804352A>G , CM000663.2:g.210804352A>G	GRCh38
NC_000001.10:g.210977694A>G , CM000663.1:g.210977694A>G	GRCh37
NC_000001.9:g.209044317A>G	NCBI36
NG_029777.1:g.334764T>C
NG_029777.2:g.334764T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271751.10:c.1463-186T>C MANE Select	ENSP00000271751.4:n.1463-186T>C
ENST00000367007.5:c.1382-186T>C	ENSP00000355974.5:n.1382-186T>C
ENST00000638357.1:c.796-186T>C
ENST00000638498.1:c.1463-186T>C	ENSP00000490983.1:n.1463-186T>C
ENST00000638960.1:c.1382-186T>C	ENSP00000492302.1:n.1382-186T>C
ENST00000639952.1:c.1382-186T>C	ENSP00000492697.1:n.1382-186T>C
ENST00000640044.1:c.311-186T>C	ENSP00000491434.1:n.311-186T>C
ENST00000640243.1:c.952-186T>C	ENSP00000492803.1:n.952-186T>C
ENST00000640522.1:c.1033-186T>C	ENSP00000491019.1:n.1033-186T>C
ENST00000640528.1:c.1382-186T>C	ENSP00000491725.1:n.1382-186T>C
ENST00000640566.1:c.311-28808T>C	ENSP00000491302.1:n.311-28808T>C
ENST00000640710.1:c.1382-186T>C	ENSP00000492513.1:n.1382-186T>C
ENST00000271751.8:c.1463-186T>C	ENSP00000271751.4:n.1463-186T>C
ENST00000367007.4:c.1382-186T>C	ENSP00000355974.4:n.1382-186T>C
NM_002238.3:c.1382-186T>C	NP_002229.1:n.1382-186T>C
NM_172362.2:c.1463-186T>C	NP_758872.1:n.1463-186T>C
XM_011509514.1:c.287-186T>C	XP_011507816.1:n.287-186T>C
XM_017001246.1:c.287-186T>C	XP_016856735.1:n.287-186T>C
NM_172362.3:c.1463-186T>C MANE Select	NP_758872.1:n.1463-186T>C
NM_002238.4:c.1382-186T>C	NP_002229.1:n.1382-186T>C