Canonical Allele Identifier: CA379133849

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2606503A>C (hg19) ; chr11:g.2585273A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2585273A>C , CM000673.2:g.2585273A>C	GRCh38
NC_000011.9:g.2606503A>C , CM000673.1:g.2606503A>C	GRCh37
NC_000011.8:g.2563079A>C	NCBI36
NG_008935.1:g.145283A>C , LRG_287:g.145283A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.771+1728A>C	ENSP00000434560.2:n.771+1728A>C
ENST00000646564.2:c.588+1728A>C	ENSP00000495806.2:n.588+1728A>C
ENST00000155840.12:c.1094A>C MANE Select	ENSP00000155840.2:p.Asn365Thr
ENST00000335475.6:c.713A>C	ENSP00000334497.5:p.Asn238Thr
ENST00000646564.1:c.234+1728A>C	ENSP00000495806.1:n.234+1728A>C
ENST00000155840.9:c.1094A>C	ENSP00000155840.2:p.Asn365Thr
ENST00000335475.5:c.713A>C	ENSP00000334497.5:p.Asn238Thr
NM_000218.2:c.1094A>C , LRG_287t1:c.1094A>C	NP_000209.2:p.Asn365Thr
NM_181798.1:c.713A>C , LRG_287t2:c.713A>C	NP_861463.1:p.Asn238Thr
NM_000218.3:c.1094A>C MANE Select	NP_000209.2:p.Asn365Thr