Canonical Allele Identifier: CA006491
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 53020
ClinVar RCV Id: RCV001841639
dbSNP Id: rs397508101

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2847814_2847816del , CM000673.2:g.2847814_2847816del GRCh38
NC_000011.9:g.2869044_2869046del , CM000673.1:g.2869044_2869046del GRCh37
NC_000011.8:g.2825620_2825622del NCBI36
NG_008935.1:g.407824_407826del , LRG_287:g.407824_407826del

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1485_1487del (KCNQ1) ENSP00000434560.2:p.His495del
ENST00000155840.12:c.1842_1844del (KCNQ1) MANE Select ENSP00000155840.2:p.His614del
ENST00000335475.6:c.1461_1463del (KCNQ1) ENSP00000334497.5:p.His487del
ENST00000526095.2:c.246_248del (KCNQ1) ENSP00000494939.1:p.His82del
ENST00000155840.9:c.1842_1844del (KCNQ1) ENSP00000155840.2:p.His614del
ENST00000335475.5:c.1461_1463del (KCNQ1) ENSP00000334497.5:p.His487del
ENST00000526095.1:n.349_351del (KCNQ1)
NM_000218.2:c.1842_1844del , LRG_287t1:c.1842_1844del (KCNQ1) NP_000209.2:p.His614del
NM_181798.1:c.1461_1463del , LRG_287t2:c.1461_1463del (KCNQ1) NP_861463.1:p.His487del
NR_130721.1:n.778-7372_778-7370del (KCNQ1-AS1)
NM_000218.3:c.1842_1844del (KCNQ1) MANE Select NP_000209.2:p.His614del