Canonical Allele Identifier: CA379117800
Gene: KCNQ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.2466702A>C (hg19) chr11:g.2445472A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445472A>C , CM000673.2:g.2445472A>C GRCh38
NC_000011.9:g.2466702A>C , CM000673.1:g.2466702A>C GRCh37
NC_000011.8:g.2423278A>C NCBI36
NG_008935.1:g.5482A>C , LRG_287:g.5482A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.113A>C ENSP00000434560.2:p.Tyr38Ser
ENST00000646564.2:c.374A>C ENSP00000495806.2:p.Tyr125Ser
ENST00000155840.12:c.374A>C MANE Select ENSP00000155840.2:p.Tyr125Ser
ENST00000646564.1:c.20A>C ENSP00000495806.1:p.Tyr7Ser
ENST00000155840.9:c.374A>C ENSP00000155840.2:p.Tyr125Ser
ENST00000345015.4:n.151A>C
ENST00000496887.6:c.113A>C ENSP00000434560.1:p.Tyr38Ser
NM_000218.2:c.374A>C , LRG_287t1:c.374A>C NP_000209.2:p.Tyr125Ser
NM_000218.3:c.374A>C MANE Select NP_000209.2:p.Tyr125Ser
Search 100 bp 5'
Search 100 bp 3'