Canonical Allele Identifier: CA375512177

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138667178A>G (hg19) ; chr9:g.135775332A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775332A>G , CM000671.2:g.135775332A>G	GRCh38
NC_000009.11:g.138667178A>G , CM000671.1:g.138667178A>G	GRCh37
NC_000009.10:g.137806999A>G	NCBI36
NG_033070.1:g.78148A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2266A>G MANE Select	ENSP00000360822.2:p.Asn756Asp
ENST00000674572.1:c.2107A>G	ENSP00000501742.1:p.Asn703Asp
ENST00000675090.1:c.2014A>G	ENSP00000501833.1:p.Asn672Asp
ENST00000675399.1:c.2014A>G	ENSP00000501932.1:p.Asn672Asp
ENST00000676421.1:c.2023A>G	ENSP00000502322.1:p.Asn675Asp
ENST00000263604.5:c.2167A>G	ENSP00000263604.4:p.Asn723Asp
ENST00000371757.6:c.2266A>G	ENSP00000360822.2:p.Asn756Asp
ENST00000460750.5:c.*1876A>G	ENSP00000418777.1:n.*1876A>G
ENST00000486577.6:c.2149A>G	ENSP00000417578.3:p.Asn717Asp
ENST00000487664.5:c.2266A>G	ENSP00000417851.2:p.Asn756Asp
ENST00000488444.6:c.2209A>G	ENSP00000419007.3:p.Asn737Asp
ENST00000490355.6:c.2203A>G	ENSP00000418003.3:p.Asn735Asp
ENST00000490363.3:n.2085A>G
ENST00000491806.6:c.2209A>G	ENSP00000419086.3:p.Asn737Asp
ENST00000628528.2:c.2131A>G	ENSP00000486374.1:p.Asn711Asp
ENST00000630792.2:c.2101A>G	ENSP00000486486.1:p.Asn701Asp
ENST00000631073.2:c.2209A>G	ENSP00000486130.1:p.Asn737Asp
ENST00000631193.1:c.115A>G	ENSP00000486830.1:p.Asn39Asp
NM_001272003.1:c.2131A>G	NP_001258932.1:p.Asn711Asp
NM_020822.2:c.2266A>G	NP_065873.2:p.Asn756Asp
XM_011518877.1:c.2401A>G	XP_011517179.1:p.Asn801Asp
XM_011518878.1:c.2410A>G	XP_011517180.1:p.Asn804Asp
XM_011518879.1:c.2401A>G	XP_011517181.1:p.Asn801Asp
XM_011518880.1:c.2167A>G	XP_011517182.1:p.Asn723Asp
XM_011518881.1:c.1756A>G	XP_011517183.1:p.Asn586Asp
XM_011518877.3:c.2401A>G	XP_011517179.1:p.Asn801Asp
XM_011518878.3:c.2410A>G	XP_011517180.1:p.Asn804Asp
XM_011518879.3:c.2401A>G	XP_011517181.1:p.Asn801Asp
XM_011518881.3:c.1756A>G	XP_011517183.1:p.Asn586Asp
XM_017014931.1:c.2200A>G	XP_016870420.1:p.Asn734Asp
XM_017014932.1:c.2023A>G	XP_016870421.1:p.Asn675Asp
XM_017014933.1:c.1756A>G	XP_016870422.1:p.Asn586Asp
XM_024447617.1:c.1756A>G	XP_024303385.1:p.Asn586Asp
XM_024447618.1:c.1756A>G	XP_024303386.1:p.Asn586Asp
NM_020822.3:c.2266A>G MANE Select	NP_065873.2:p.Asn756Asp
NM_001272003.2:c.2131A>G	NP_001258932.1:p.Asn711Asp