Canonical Allele Identifier: CA379121925

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2549214A>T (hg19) ; chr11:g.2527984A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2527984A>T , CM000673.2:g.2527984A>T	GRCh38
NC_000011.9:g.2549214A>T , CM000673.1:g.2549214A>T	GRCh37
NC_000011.8:g.2505790A>T	NCBI36
NG_008935.1:g.87994A>T , LRG_287:g.87994A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.182A>T	ENSP00000434560.2:p.Tyr61Phe
ENST00000646564.2:c.443A>T	ENSP00000495806.2:p.Tyr148Phe
ENST00000155840.12:c.443A>T MANE Select	ENSP00000155840.2:p.Tyr148Phe
ENST00000335475.6:c.62A>T	ENSP00000334497.5:p.Tyr21Phe
ENST00000646564.1:c.89A>T	ENSP00000495806.1:p.Tyr30Phe
ENST00000155840.9:c.443A>T	ENSP00000155840.2:p.Tyr148Phe
ENST00000335475.5:c.62A>T	ENSP00000334497.5:p.Tyr21Phe
ENST00000496887.6:c.182A>T	ENSP00000434560.1:p.Tyr61Phe
NM_000218.2:c.443A>T , LRG_287t1:c.443A>T	NP_000209.2:p.Tyr148Phe
NM_181798.1:c.62A>T , LRG_287t2:c.62A>T	NP_861463.1:p.Tyr21Phe
NM_000218.3:c.443A>T MANE Select	NP_000209.2:p.Tyr148Phe