Canonical Allele Identifier: CA379131658

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2594185G>C (hg19) ; chr11:g.2572955G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572955G>C , CM000673.2:g.2572955G>C	GRCh38
NC_000011.9:g.2594185G>C , CM000673.1:g.2594185G>C	GRCh37
NC_000011.8:g.2550761G>C	NCBI36
NG_008935.1:g.132965G>C , LRG_287:g.132965G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.629G>C	ENSP00000434560.2:p.Gly210Ala
ENST00000646564.2:c.478-10480G>C	ENSP00000495806.2:n.478-10480G>C
ENST00000155840.12:c.890G>C MANE Select	ENSP00000155840.2:p.Gly297Ala
ENST00000335475.6:c.509G>C	ENSP00000334497.5:p.Gly170Ala
ENST00000646564.1:c.124-10480G>C	ENSP00000495806.1:n.124-10480G>C
ENST00000155840.9:c.890G>C	ENSP00000155840.2:p.Gly297Ala
ENST00000335475.5:c.509G>C	ENSP00000334497.5:p.Gly170Ala
NM_000218.2:c.890G>C , LRG_287t1:c.890G>C	NP_000209.2:p.Gly297Ala
NM_181798.1:c.509G>C , LRG_287t2:c.509G>C	NP_861463.1:p.Gly170Ala
NM_000218.3:c.890G>C MANE Select	NP_000209.2:p.Gly297Ala