Canonical Allele Identifier: CA379135226

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1484839840
• gnomAD v2: 11-2610081-T-C
• gnomAD v4: 11-2588851-T-C
• MyVariant Identifiers: chr11:g.2610081T>C (hg19) ; chr11:g.2588851T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2588851T>C , CM000673.2:g.2588851T>C	GRCh38
NC_000011.9:g.2610081T>C , CM000673.1:g.2610081T>C	GRCh37
NC_000011.8:g.2566657T>C	NCBI36
NG_008935.1:g.148861T>C , LRG_287:g.148861T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1033T>C	ENSP00000434560.2:p.Ser345Pro
ENST00000646564.2:c.850T>C	ENSP00000495806.2:p.Ser284Pro
ENST00000155840.12:c.1390T>C MANE Select	ENSP00000155840.2:p.Ser464Pro
ENST00000335475.6:c.1009T>C	ENSP00000334497.5:p.Ser337Pro
ENST00000646564.1:c.496T>C	ENSP00000495806.1:p.Ser166Pro
ENST00000155840.9:c.1390T>C	ENSP00000155840.2:p.Ser464Pro
ENST00000335475.5:c.1009T>C	ENSP00000334497.5:p.Ser337Pro
NM_000218.2:c.1390T>C , LRG_287t1:c.1390T>C	NP_000209.2:p.Ser464Pro
NM_181798.1:c.1009T>C , LRG_287t2:c.1009T>C	NP_861463.1:p.Ser337Pro
NM_000218.3:c.1390T>C MANE Select	NP_000209.2:p.Ser464Pro