Canonical Allele Identifier: CA2612002357
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583303_2583304del , CM000673.2:g.2583303_2583304del GRCh38
NC_000011.9:g.2604533_2604534del , CM000673.1:g.2604533_2604534del GRCh37
NC_000011.8:g.2561109_2561110del NCBI36
NG_008935.1:g.143313_143314del , LRG_287:g.143313_143314del

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.661-132_661-131del ENSP00000434560.2:n.661-132_661-131del
ENST00000646564.2:c.478-132_478-131del ENSP00000495806.2:n.478-132_478-131del
ENST00000155840.12:c.922-132_922-131del MANE Select ENSP00000155840.2:n.922-132_922-131del
ENST00000335475.6:c.541-132_541-131del ENSP00000334497.5:n.541-132_541-131del
ENST00000646564.1:c.124-132_124-131del ENSP00000495806.1:n.124-132_124-131del
ENST00000155840.9:c.922-132_922-131del ENSP00000155840.2:n.922-132_922-131del
ENST00000335475.5:c.541-132_541-131del ENSP00000334497.5:n.541-132_541-131del
NM_000218.2:c.922-132_922-131del , LRG_287t1:c.922-132_922-131del NP_000209.2:n.922-132_922-131del
NM_181798.1:c.541-132_541-131del , LRG_287t2:c.541-132_541-131del NP_861463.1:n.541-132_541-131del
NM_000218.3:c.922-132_922-131del MANE Select NP_000209.2:n.922-132_922-131del