Canonical Allele Identifier: CA2612011947

Gene: KCNQ1 KCNQ1-AS1

Linked Data

• gnomAD v4: 11-2848416-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2848416A>T , CM000673.2:g.2848416A>T	GRCh38
NC_000011.9:g.2869646A>T , CM000673.1:g.2869646A>T	GRCh37
NC_000011.8:g.2826222A>T	NCBI36
NG_008935.1:g.408426A>T , LRG_287:g.408426A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.*413A>T (KCNQ1)	ENSP00000434560.2:n.*413A>T
ENST00000155840.12:c.*413A>T (KCNQ1) MANE Select	ENSP00000155840.2:n.*413A>T
ENST00000335475.6:c.*413A>T (KCNQ1)	ENSP00000334497.5:n.*413A>T
ENST00000155840.9:c.*413A>T (KCNQ1)	ENSP00000155840.2:n.*413A>T
ENST00000526095.1:n.951A>T (KCNQ1)
NM_000218.2:c.*413A>T , LRG_287t1:c.*413A>T (KCNQ1)	NP_000209.2:n.*413A>T
NM_181798.1:c.*413A>T , LRG_287t2:c.*413A>T (KCNQ1)	NP_861463.1:n.*413A>T
NR_130721.1:n.778-7974T>A (KCNQ1-AS1)
NM_000218.3:c.*413A>T (KCNQ1) MANE Select	NP_000209.2:n.*413A>T