Canonical Allele Identifier: CA2612011410
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2847878del , CM000673.2:g.2847878del GRCh38
NC_000011.9:g.2869108del , CM000673.1:g.2869108del GRCh37
NC_000011.8:g.2825684del NCBI36
NG_008935.1:g.407888del , LRG_287:g.407888del

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1549del (KCNQ1) ENSP00000434560.2:p.Ala517ProfsTer30
ENST00000155840.12:c.1906del (KCNQ1) MANE Select ENSP00000155840.2:p.Ala636ProfsTer30
ENST00000335475.6:c.1525del (KCNQ1) ENSP00000334497.5:p.Ala509ProfsTer30
ENST00000526095.2:c.310del (KCNQ1) ENSP00000494939.1:p.Ala104ProfsTer30
ENST00000155840.9:c.1906del (KCNQ1) ENSP00000155840.2:p.Ala636ProfsTer30
ENST00000335475.5:c.1525del (KCNQ1) ENSP00000334497.5:p.Ala509ProfsTer30
ENST00000526095.1:n.413del (KCNQ1)
NM_000218.2:c.1906del , LRG_287t1:c.1906del (KCNQ1) NP_000209.2:p.Ala636ProfsTer30
NM_181798.1:c.1525del , LRG_287t2:c.1525del (KCNQ1) NP_861463.1:p.Ala509ProfsTer30
NR_130721.1:n.778-7433del (KCNQ1-AS1)
NM_000218.3:c.1906del (KCNQ1) MANE Select NP_000209.2:p.Ala636ProfsTer30