Canonical Allele Identifier: CA2612010956

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2777955-T-TCTATGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2777955_2777956insCTATGGG , CM000673.2:g.2777955_2777956insCTATGGG	GRCh38
NC_000011.9:g.2799185_2799186insCTATGGG , CM000673.1:g.2799185_2799186insCTATGGG	GRCh37
NC_000011.8:g.2755761_2755762insCTATGGG	NCBI36
NG_008935.1:g.337965_337966insCTATGGG , LRG_287:g.337965_337966insCTATGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1376-21_1376-20insCTATGGG	ENSP00000434560.2:n.1376-21_1376-20insCTATGGG
ENST00000646564.2:c.1193-21_1193-20insCTATGGG	ENSP00000495806.2:n.1193-21_1193-20insCTATGGG
ENST00000155840.12:c.1733-21_1733-20insCTATGGG MANE Select	ENSP00000155840.2:n.1733-21_1733-20insCTATGGG
ENST00000335475.6:c.1352-21_1352-20insCTATGGG	ENSP00000334497.5:n.1352-21_1352-20insCTATGGG
ENST00000526095.2:c.137-21_137-20insCTATGGG	ENSP00000494939.1:n.137-21_137-20insCTATGGG
ENST00000646564.1:c.839-21_839-20insCTATGGG	ENSP00000495806.1:n.839-21_839-20insCTATGGG
ENST00000155840.9:c.1733-21_1733-20insCTATGGG	ENSP00000155840.2:n.1733-21_1733-20insCTATGGG
ENST00000335475.5:c.1352-21_1352-20insCTATGGG	ENSP00000334497.5:n.1352-21_1352-20insCTATGGG
ENST00000526095.1:n.240-21_240-20insCTATGGG
NM_000218.2:c.1733-21_1733-20insCTATGGG , LRG_287t1:c.1733-21_1733-20insCTATGGG	NP_000209.2:n.1733-21_1733-20insCTATGGG
NM_181798.1:c.1352-21_1352-20insCTATGGG , LRG_287t2:c.1352-21_1352-20insCTATGGG	NP_861463.1:n.1352-21_1352-20insCTATGGG
NM_000218.3:c.1733-21_1733-20insCTATGGG MANE Select	NP_000209.2:n.1733-21_1733-20insCTATGGG