Canonical Allele Identifier: CA1883873673

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770445_135770449delinsGAAGT , CM000671.2:g.135770445_135770449delinsGAAGT	GRCh38
NC_000009.11:g.138662291_138662295delinsGAAGT , CM000671.1:g.138662291_138662295delinsGAAGT	GRCh37
NC_000009.10:g.137802112_137802116delinsGAAGT	NCBI36
NG_033070.1:g.73261_73265delinsGAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1767_1769+2delinsGAAGT
ENST00000674572.1:c.1608_1610+2delinsGAAGT
ENST00000675090.1:c.1515_1517+2delinsGAAGT
ENST00000675399.1:c.1515_1517+2delinsGAAGT
ENST00000676421.1:c.1524_1526+2delinsGAAGT
ENST00000263604.5:c.1668_1670+2delinsGAAGT
ENST00000371757.6:c.1767_1769+2delinsGAAGT
ENST00000460750.5:c.*1377_*1379+2delinsGAAGT
ENST00000486577.6:c.1650_1652+2delinsGAAGT
ENST00000487664.5:c.1767_1769+2delinsGAAGT
ENST00000488444.6:c.1710_1712+2delinsGAAGT
ENST00000490355.6:c.1710_1712+2delinsGAAGT
ENST00000490363.3:n.1586_1588+2delinsGAAGT
ENST00000491806.6:c.1710_1712+2delinsGAAGT
ENST00000628528.2:c.1632_1634+2delinsGAAGT
ENST00000630792.2:c.1608_1610+2delinsGAAGT
ENST00000631073.2:c.1710_1712+2delinsGAAGT
NM_001272003.1:c.1632_1634+2delinsGAAGT
NM_020822.2:c.1767_1769+2delinsGAAGT
XM_011518877.1:c.1902_1904+2delinsGAAGT
XM_011518878.1:c.1911_1913+2delinsGAAGT
XM_011518879.1:c.1902_1904+2delinsGAAGT
XM_011518880.1:c.1668_1670+2delinsGAAGT
XM_011518881.1:c.1257_1259+2delinsGAAGT
XM_011518877.3:c.1902_1904+2delinsGAAGT
XM_011518878.3:c.1911_1913+2delinsGAAGT
XM_011518879.3:c.1902_1904+2delinsGAAGT
XM_011518881.3:c.1257_1259+2delinsGAAGT
XM_017014931.1:c.1701_1703+2delinsGAAGT
XM_017014932.1:c.1524_1526+2delinsGAAGT
XM_017014933.1:c.1257_1259+2delinsGAAGT
XM_024447617.1:c.1257_1259+2delinsGAAGT
XM_024447618.1:c.1257_1259+2delinsGAAGT
NM_020822.3:c.1767_1769+2delinsGAAGT
NM_001272003.2:c.1632_1634+2delinsGAAGT