Canonical Allele Identifier: CA1948243170

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572858_2572859delinsAC , CM000673.2:g.2572858_2572859delinsAC	GRCh38
NC_000011.9:g.2594088_2594089delinsAC , CM000673.1:g.2594088_2594089delinsAC	GRCh37
NC_000011.8:g.2550664_2550665delinsAC	NCBI36
NG_008935.1:g.132868_132869delinsAC , LRG_287:g.132868_132869delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.532_533delinsAC	ENSP00000434560.2:p.Thr178=
ENST00000646564.2:c.478-10577_478-10576delinsAC	ENSP00000495806.2:n.478-10577_478-10576delinsAC
ENST00000155840.12:c.793_794delinsAC MANE Select	ENSP00000155840.2:p.Thr265=
ENST00000335475.6:c.412_413delinsAC	ENSP00000334497.5:p.Thr138=
ENST00000646564.1:c.124-10577_124-10576delinsAC	ENSP00000495806.1:n.124-10577_124-10576delinsAC
ENST00000155840.9:c.793_794delinsAC	ENSP00000155840.2:p.Thr265=
ENST00000335475.5:c.412_413delinsAC	ENSP00000334497.5:p.Thr138=
ENST00000496887.6:c.532_533delinsAC	ENSP00000434560.1:p.Thr178=
NM_000218.2:c.793_794delinsAC , LRG_287t1:c.793_794delinsAC	NP_000209.2:p.Thr265=
NM_181798.1:c.412_413delinsAC , LRG_287t2:c.412_413delinsAC	NP_861463.1:p.Thr138=
NM_000218.3:c.793_794delinsAC MANE Select	NP_000209.2:p.Thr265=