Canonical Allele Identifier: CA2579511256

Gene: KCNT1

Linked Data

• gnomAD v4: 9-135775247-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775251del , CM000671.2:g.135775251del	GRCh38
NC_000009.11:g.138667097del , CM000671.1:g.138667097del	GRCh37
NC_000009.10:g.137806918del	NCBI36
NG_033070.1:g.78067del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.2244-59del MANE Select	ENSP00000360822.2:n.2244-59del
ENST00000674572.1:c.2085-59del	ENSP00000501742.1:n.2085-59del
ENST00000675090.1:c.1992-59del	ENSP00000501833.1:n.1992-59del
ENST00000675399.1:c.1992-59del	ENSP00000501932.1:n.1992-59del
ENST00000676421.1:c.2001-59del	ENSP00000502322.1:n.2001-59del
ENST00000263604.5:c.2145-59del	ENSP00000263604.4:n.2145-59del
ENST00000371757.6:c.2244-59del	ENSP00000360822.2:n.2244-59del
ENST00000460750.5:c.*1854-59del	ENSP00000418777.1:n.*1854-59del
ENST00000486577.6:c.2127-59del	ENSP00000417578.3:n.2127-59del
ENST00000487664.5:c.2244-59del	ENSP00000417851.2:n.2244-59del
ENST00000488444.6:c.2187-59del	ENSP00000419007.3:n.2187-59del
ENST00000490355.6:c.2181-59del	ENSP00000418003.3:n.2181-59del
ENST00000490363.3:n.2063-59del
ENST00000491806.6:c.2187-59del	ENSP00000419086.3:n.2187-59del
ENST00000628528.2:c.2109-59del	ENSP00000486374.1:n.2109-59del
ENST00000630792.2:c.2079-59del	ENSP00000486486.1:n.2079-59del
ENST00000631073.2:c.2187-59del	ENSP00000486130.1:n.2187-59del
ENST00000631193.1:c.93-59del	ENSP00000486830.1:n.93-59del
NM_001272003.1:c.2109-59del	NP_001258932.1:n.2109-59del
NM_020822.2:c.2244-59del	NP_065873.2:n.2244-59del
XM_011518877.1:c.2379-59del	XP_011517179.1:n.2379-59del
XM_011518878.1:c.2388-59del	XP_011517180.1:n.2388-59del
XM_011518879.1:c.2379-59del	XP_011517181.1:n.2379-59del
XM_011518880.1:c.2145-59del	XP_011517182.1:n.2145-59del
XM_011518881.1:c.1734-59del	XP_011517183.1:n.1734-59del
XM_011518877.3:c.2379-59del	XP_011517179.1:n.2379-59del
XM_011518878.3:c.2388-59del	XP_011517180.1:n.2388-59del
XM_011518879.3:c.2379-59del	XP_011517181.1:n.2379-59del
XM_011518881.3:c.1734-59del	XP_011517183.1:n.1734-59del
XM_017014931.1:c.2178-59del	XP_016870420.1:n.2178-59del
XM_017014932.1:c.2001-59del	XP_016870421.1:n.2001-59del
XM_017014933.1:c.1734-59del	XP_016870422.1:n.1734-59del
XM_024447617.1:c.1734-59del	XP_024303385.1:n.1734-59del
XM_024447618.1:c.1734-59del	XP_024303386.1:n.1734-59del
NM_020822.3:c.2244-59del MANE Select	NP_065873.2:n.2244-59del
NM_001272003.2:c.2109-59del	NP_001258932.1:n.2109-59del