Canonical Allele Identifier: CA2612008568
Gene: KCNQ1 HGNC NCBI

Linked Data

gnomAD v4: 11-2775916-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2775916G>A , CM000673.2:g.2775916G>A GRCh38
NC_000011.9:g.2797146G>A , CM000673.1:g.2797146G>A GRCh37
NC_000011.8:g.2753722G>A NCBI36
NG_008935.1:g.335926G>A , LRG_287:g.335926G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.1234-44G>A ENSP00000434560.2:n.1234-44G>A
ENST00000646564.2:c.1051-44G>A ENSP00000495806.2:n.1051-44G>A
ENST00000155840.12:c.1591-44G>A MANE Select ENSP00000155840.2:n.1591-44G>A
ENST00000335475.6:c.1210-44G>A ENSP00000334497.5:n.1210-44G>A
ENST00000646564.1:c.697-44G>A ENSP00000495806.1:n.697-44G>A
ENST00000155840.9:c.1591-44G>A ENSP00000155840.2:n.1591-44G>A
ENST00000335475.5:c.1210-44G>A ENSP00000334497.5:n.1210-44G>A
NM_000218.2:c.1591-44G>A , LRG_287t1:c.1591-44G>A NP_000209.2:n.1591-44G>A
NM_181798.1:c.1210-44G>A , LRG_287t2:c.1210-44G>A NP_861463.1:n.1210-44G>A
NM_000218.3:c.1591-44G>A MANE Select NP_000209.2:n.1591-44G>A
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