Canonical Allele Identifier: CA1948349530
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2847691A= , CM000673.2:g.2847691A= GRCh38
NC_000011.9:g.2868921A= , CM000673.1:g.2868921A= GRCh37
NC_000011.8:g.2825497A= NCBI36
NG_008935.1:g.407701A= , LRG_287:g.407701A=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1438-76A= (KCNQ1) ENSP00000434560.2:n.1438-76A=
ENST00000155840.12:c.1795-76A= (KCNQ1) MANE Select ENSP00000155840.2:n.1795-76A=
ENST00000335475.6:c.1414-76A= (KCNQ1) ENSP00000334497.5:n.1414-76A=
ENST00000526095.2:c.199-76A= (KCNQ1) ENSP00000494939.1:n.199-76A=
ENST00000155840.9:c.1795-76A= (KCNQ1) ENSP00000155840.2:n.1795-76A=
ENST00000335475.5:c.1414-76A= (KCNQ1) ENSP00000334497.5:n.1414-76A=
ENST00000526095.1:n.302-76A= (KCNQ1)
NM_000218.2:c.1795-76A= , LRG_287t1:c.1795-76A= (KCNQ1) NP_000209.2:n.1795-76A=
NM_181798.1:c.1414-76A= , LRG_287t2:c.1414-76A= (KCNQ1) NP_861463.1:n.1414-76A=
NR_130721.1:n.778-7249T= (KCNQ1-AS1)
NM_000218.3:c.1795-76A= (KCNQ1) MANE Select NP_000209.2:n.1795-76A=
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