Canonical Allele Identifier: CA675202385
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1251203261
MyVariant Identifiers: chr11:g.2869660G>A (hg19) chr11:g.2848430G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2848430G>A , CM000673.2:g.2848430G>A GRCh38
NC_000011.9:g.2869660G>A , CM000673.1:g.2869660G>A GRCh37
NC_000011.8:g.2826236G>A NCBI36
NG_008935.1:g.408440G>A , LRG_287:g.408440G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.*427G>A (KCNQ1) ENSP00000434560.2:n.*427G>A
ENST00000155840.12:c.*427G>A (KCNQ1) MANE Select ENSP00000155840.2:n.*427G>A
ENST00000335475.6:c.*427G>A (KCNQ1) ENSP00000334497.5:n.*427G>A
ENST00000155840.9:c.*427G>A (KCNQ1) ENSP00000155840.2:n.*427G>A
ENST00000526095.1:n.965G>A (KCNQ1)
NM_000218.2:c.*427G>A , LRG_287t1:c.*427G>A (KCNQ1) NP_000209.2:n.*427G>A
NM_181798.1:c.*427G>A , LRG_287t2:c.*427G>A (KCNQ1) NP_861463.1:n.*427G>A
NR_130721.1:n.778-7988C>T (KCNQ1-AS1)
NM_000218.3:c.*427G>A (KCNQ1) MANE Select NP_000209.2:n.*427G>A
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