Canonical Allele Identifier: CA1948243191
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572885A= , CM000673.2:g.2572885A= GRCh38
NC_000011.9:g.2594115A= , CM000673.1:g.2594115A= GRCh37
NC_000011.8:g.2550691A= NCBI36
NG_008935.1:g.132895A= , LRG_287:g.132895A=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.559A= ENSP00000434560.2:p.Ile187=
ENST00000646564.2:c.478-10550A= ENSP00000495806.2:n.478-10550A=
ENST00000155840.12:c.820A= MANE Select ENSP00000155840.2:p.Ile274=
ENST00000335475.6:c.439A= ENSP00000334497.5:p.Ile147=
ENST00000646564.1:c.124-10550A= ENSP00000495806.1:n.124-10550A=
ENST00000155840.9:c.820A= ENSP00000155840.2:p.Ile274=
ENST00000335475.5:c.439A= ENSP00000334497.5:p.Ile147=
ENST00000496887.6:c.559A= ENSP00000434560.1:p.Ile187=
NM_000218.2:c.820A= , LRG_287t1:c.820A= NP_000209.2:p.Ile274=
NM_181798.1:c.439A= , LRG_287t2:c.439A= NP_861463.1:p.Ile147=
NM_000218.3:c.820A= MANE Select NP_000209.2:p.Ile274=