Canonical Allele Identifier: CA2612010761

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2777808-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2777808C>T , CM000673.2:g.2777808C>T	GRCh38
NC_000011.9:g.2799038C>T , CM000673.1:g.2799038C>T	GRCh37
NC_000011.8:g.2755614C>T	NCBI36
NG_008935.1:g.337818C>T , LRG_287:g.337818C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1376-168C>T	ENSP00000434560.2:n.1376-168C>T
ENST00000646564.2:c.1193-168C>T	ENSP00000495806.2:n.1193-168C>T
ENST00000155840.12:c.1733-168C>T MANE Select	ENSP00000155840.2:n.1733-168C>T
ENST00000335475.6:c.1352-168C>T	ENSP00000334497.5:n.1352-168C>T
ENST00000526095.2:c.131C>T	ENSP00000494939.1:p.Thr44Ile
ENST00000646564.1:c.839-168C>T	ENSP00000495806.1:n.839-168C>T
ENST00000155840.9:c.1733-168C>T	ENSP00000155840.2:n.1733-168C>T
ENST00000335475.5:c.1352-168C>T	ENSP00000334497.5:n.1352-168C>T
ENST00000526095.1:n.234C>T
NM_000218.2:c.1733-168C>T , LRG_287t1:c.1733-168C>T	NP_000209.2:n.1733-168C>T
NM_181798.1:c.1352-168C>T , LRG_287t2:c.1352-168C>T	NP_861463.1:n.1352-168C>T
NM_000218.3:c.1733-168C>T MANE Select	NP_000209.2:n.1733-168C>T