Canonical Allele Identifier: CA379132962

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2604674A>C (hg19) ; chr11:g.2583444A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583444A>C , CM000673.2:g.2583444A>C	GRCh38
NC_000011.9:g.2604674A>C , CM000673.1:g.2604674A>C	GRCh37
NC_000011.8:g.2561250A>C	NCBI36
NG_008935.1:g.143454A>C , LRG_287:g.143454A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.670A>C	ENSP00000434560.2:p.Thr224Pro
ENST00000646564.2:c.487A>C	ENSP00000495806.2:p.Thr163Pro
ENST00000155840.12:c.931A>C MANE Select	ENSP00000155840.2:p.Thr311Pro
ENST00000335475.6:c.550A>C	ENSP00000334497.5:p.Thr184Pro
ENST00000646564.1:c.133A>C	ENSP00000495806.1:p.Thr45Pro
ENST00000155840.9:c.931A>C	ENSP00000155840.2:p.Thr311Pro
ENST00000335475.5:c.550A>C	ENSP00000334497.5:p.Thr184Pro
NM_000218.2:c.931A>C , LRG_287t1:c.931A>C	NP_000209.2:p.Thr311Pro
NM_181798.1:c.550A>C , LRG_287t2:c.550A>C	NP_861463.1:p.Thr184Pro
NM_000218.3:c.931A>C MANE Select	NP_000209.2:p.Thr311Pro