Canonical Allele Identifier: CA2840352985

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2528097_2528098del , CM000673.2:g.2528097_2528098del	GRCh38
NC_000011.9:g.2549327_2549328del , CM000673.1:g.2549327_2549328del	GRCh37
NC_000011.8:g.2505903_2505904del	NCBI36
NG_008935.1:g.88107_88108del , LRG_287:g.88107_88108del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.216+79_216+80del	ENSP00000434560.2:n.216+79_216+80del
ENST00000646564.2:c.477+79_477+80del	ENSP00000495806.2:n.477+79_477+80del
ENST00000155840.12:c.477+79_477+80del MANE Select	ENSP00000155840.2:n.477+79_477+80del
ENST00000335475.6:c.96+79_96+80del	ENSP00000334497.5:n.96+79_96+80del
ENST00000646564.1:c.123+79_123+80del	ENSP00000495806.1:n.123+79_123+80del
ENST00000155840.9:c.477+79_477+80del	ENSP00000155840.2:n.477+79_477+80del
ENST00000335475.5:c.96+79_96+80del	ENSP00000334497.5:n.96+79_96+80del
ENST00000496887.6:c.216+79_216+80del	ENSP00000434560.1:n.216+79_216+80del
NM_000218.2:c.477+79_477+80del , LRG_287t1:c.477+79_477+80del	NP_000209.2:n.477+79_477+80del
NM_181798.1:c.96+79_96+80del , LRG_287t2:c.96+79_96+80del	NP_861463.1:n.96+79_96+80del
NM_000218.3:c.477+79_477+80del MANE Select	NP_000209.2:n.477+79_477+80del