Canonical Allele Identifier: CA2574728427

Gene: KCNQ1 KCNQ1OT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2662178_2662188del , CM000673.2:g.2662178_2662188del	GRCh38
NC_000011.9:g.2683408_2683418del , CM000673.1:g.2683408_2683418del	GRCh37
NC_000011.8:g.2639984_2639994del	NCBI36
NG_008935.1:g.222188_222198del , LRG_287:g.222188_222198del
NG_016178.2:g.42811_42821del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1157+97_1157+107del (KCNQ1)	ENSP00000434560.2:n.1157+97_1157+107del
ENST00000646564.2:c.974+97_974+107del (KCNQ1)	ENSP00000495806.2:n.974+97_974+107del
ENST00000155840.12:c.1514+97_1514+107del (KCNQ1) MANE Select	ENSP00000155840.2:n.1514+97_1514+107del
ENST00000335475.6:c.1133+97_1133+107del (KCNQ1)	ENSP00000334497.5:n.1133+97_1133+107del
ENST00000646564.1:c.620+97_620+107del (KCNQ1)	ENSP00000495806.1:n.620+97_620+107del
ENST00000155840.9:c.1514+97_1514+107del (KCNQ1)	ENSP00000155840.2:n.1514+97_1514+107del
ENST00000335475.5:c.1133+97_1133+107del (KCNQ1)	ENSP00000334497.5:n.1133+97_1133+107del
NM_000218.2:c.1514+97_1514+107del , LRG_287t1:c.1514+97_1514+107del (KCNQ1)	NP_000209.2:n.1514+97_1514+107del
NM_181798.1:c.1133+97_1133+107del , LRG_287t2:c.1133+97_1133+107del (KCNQ1)	NP_861463.1:n.1133+97_1133+107del
NR_002728.3:n.37811_37821del (KCNQ1OT1)
NM_000218.3:c.1514+97_1514+107del (KCNQ1) MANE Select	NP_000209.2:n.1514+97_1514+107del