Canonical Allele Identifier: CA1948349901
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2848294C= , CM000673.2:g.2848294C= GRCh38
NC_000011.9:g.2869524C= , CM000673.1:g.2869524C= GRCh37
NC_000011.8:g.2826100C= NCBI36
NG_008935.1:g.408304C= , LRG_287:g.408304C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.*291C= (KCNQ1) ENSP00000434560.2:n.*291C=
ENST00000155840.12:c.*291C= (KCNQ1) MANE Select ENSP00000155840.2:n.*291C=
ENST00000335475.6:c.*291C= (KCNQ1) ENSP00000334497.5:n.*291C=
ENST00000155840.9:c.*291C= (KCNQ1) ENSP00000155840.2:n.*291C=
ENST00000526095.1:n.829C= (KCNQ1)
NM_000218.2:c.*291C= , LRG_287t1:c.*291C= (KCNQ1) NP_000209.2:n.*291C=
NM_181798.1:c.*291C= , LRG_287t2:c.*291C= (KCNQ1) NP_861463.1:n.*291C=
NR_130721.1:n.778-7852G= (KCNQ1-AS1)
NM_000218.3:c.*291C= (KCNQ1) MANE Select NP_000209.2:n.*291C=