Canonical Allele Identifier: CA2574728522

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2777923-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2777927del , CM000673.2:g.2777927del	GRCh38
NC_000011.9:g.2799157del , CM000673.1:g.2799157del	GRCh37
NC_000011.8:g.2755733del	NCBI36
NG_008935.1:g.337937del , LRG_287:g.337937del

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1376-49del	ENSP00000434560.2:n.1376-49del
ENST00000646564.2:c.1193-49del	ENSP00000495806.2:n.1193-49del
ENST00000155840.12:c.1733-49del MANE Select	ENSP00000155840.2:n.1733-49del
ENST00000335475.6:c.1352-49del	ENSP00000334497.5:n.1352-49del
ENST00000526095.2:c.137-49del	ENSP00000494939.1:n.137-49del
ENST00000646564.1:c.839-49del	ENSP00000495806.1:n.839-49del
ENST00000155840.9:c.1733-49del	ENSP00000155840.2:n.1733-49del
ENST00000335475.5:c.1352-49del	ENSP00000334497.5:n.1352-49del
ENST00000526095.1:n.240-49del
NM_000218.2:c.1733-49del , LRG_287t1:c.1733-49del	NP_000209.2:n.1733-49del
NM_181798.1:c.1352-49del , LRG_287t2:c.1352-49del	NP_861463.1:n.1352-49del
NM_000218.3:c.1733-49del MANE Select	NP_000209.2:n.1733-49del