Canonical Allele Identifier: CA2612011851

Gene: KCNQ1 KCNQ1-AS1

Linked Data

• gnomAD v4: 11-2848284-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2848284G>T , CM000673.2:g.2848284G>T	GRCh38
NC_000011.9:g.2869514G>T , CM000673.1:g.2869514G>T	GRCh37
NC_000011.8:g.2826090G>T	NCBI36
NG_008935.1:g.408294G>T , LRG_287:g.408294G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.*281G>T (KCNQ1)	ENSP00000434560.2:n.*281G>T
ENST00000155840.12:c.*281G>T (KCNQ1) MANE Select	ENSP00000155840.2:n.*281G>T
ENST00000335475.6:c.*281G>T (KCNQ1)	ENSP00000334497.5:n.*281G>T
ENST00000526095.2:c.*281G>T (KCNQ1)	ENSP00000494939.1:n.*281G>T
ENST00000155840.9:c.*281G>T (KCNQ1)	ENSP00000155840.2:n.*281G>T
ENST00000526095.1:n.819G>T (KCNQ1)
NM_000218.2:c.*281G>T , LRG_287t1:c.*281G>T (KCNQ1)	NP_000209.2:n.*281G>T
NM_181798.1:c.*281G>T , LRG_287t2:c.*281G>T (KCNQ1)	NP_861463.1:n.*281G>T
NR_130721.1:n.778-7842C>A (KCNQ1-AS1)
NM_000218.3:c.*281G>T (KCNQ1) MANE Select	NP_000209.2:n.*281G>T