Canonical Allele Identifier: CA5327244

Gene: KCNT1

Linked Data

• dbSNP Id: rs770294076
• ExAC: 9:138667179 A / G
• gnomAD v2: 9-138667179-A-G
• gnomAD v4: 9-135775333-A-G
• MyVariant Identifiers: chr9:g.138667179A>G (hg19) ; chr9:g.135775333A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775333A>G , CM000671.2:g.135775333A>G	GRCh38
NC_000009.11:g.138667179A>G , CM000671.1:g.138667179A>G	GRCh37
NC_000009.10:g.137807000A>G	NCBI36
NG_033070.1:g.78149A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2267A>G MANE Select	ENSP00000360822.2:p.Asn756Ser
ENST00000674572.1:c.2108A>G	ENSP00000501742.1:p.Asn703Ser
ENST00000675090.1:c.2015A>G	ENSP00000501833.1:p.Asn672Ser
ENST00000675399.1:c.2015A>G	ENSP00000501932.1:p.Asn672Ser
ENST00000676421.1:c.2024A>G	ENSP00000502322.1:p.Asn675Ser
ENST00000263604.5:c.2168A>G	ENSP00000263604.4:p.Asn723Ser
ENST00000371757.6:c.2267A>G	ENSP00000360822.2:p.Asn756Ser
ENST00000460750.5:c.*1877A>G	ENSP00000418777.1:n.*1877A>G
ENST00000486577.6:c.2150A>G	ENSP00000417578.3:p.Asn717Ser
ENST00000487664.5:c.2267A>G	ENSP00000417851.2:p.Asn756Ser
ENST00000488444.6:c.2210A>G	ENSP00000419007.3:p.Asn737Ser
ENST00000490355.6:c.2204A>G	ENSP00000418003.3:p.Asn735Ser
ENST00000490363.3:n.2086A>G
ENST00000491806.6:c.2210A>G	ENSP00000419086.3:p.Asn737Ser
ENST00000628528.2:c.2132A>G	ENSP00000486374.1:p.Asn711Ser
ENST00000630792.2:c.2102A>G	ENSP00000486486.1:p.Asn701Ser
ENST00000631073.2:c.2210A>G	ENSP00000486130.1:p.Asn737Ser
ENST00000631193.1:c.116A>G	ENSP00000486830.1:p.Asn39Ser
NM_001272003.1:c.2132A>G	NP_001258932.1:p.Asn711Ser
NM_020822.2:c.2267A>G	NP_065873.2:p.Asn756Ser
XM_011518877.1:c.2402A>G	XP_011517179.1:p.Asn801Ser
XM_011518878.1:c.2411A>G	XP_011517180.1:p.Asn804Ser
XM_011518879.1:c.2402A>G	XP_011517181.1:p.Asn801Ser
XM_011518880.1:c.2168A>G	XP_011517182.1:p.Asn723Ser
XM_011518881.1:c.1757A>G	XP_011517183.1:p.Asn586Ser
XM_011518877.3:c.2402A>G	XP_011517179.1:p.Asn801Ser
XM_011518878.3:c.2411A>G	XP_011517180.1:p.Asn804Ser
XM_011518879.3:c.2402A>G	XP_011517181.1:p.Asn801Ser
XM_011518881.3:c.1757A>G	XP_011517183.1:p.Asn586Ser
XM_017014931.1:c.2201A>G	XP_016870420.1:p.Asn734Ser
XM_017014932.1:c.2024A>G	XP_016870421.1:p.Asn675Ser
XM_017014933.1:c.1757A>G	XP_016870422.1:p.Asn586Ser
XM_024447617.1:c.1757A>G	XP_024303385.1:p.Asn586Ser
XM_024447618.1:c.1757A>G	XP_024303386.1:p.Asn586Ser
NM_020822.3:c.2267A>G MANE Select	NP_065873.2:p.Asn756Ser
NM_001272003.2:c.2132A>G	NP_001258932.1:p.Asn711Ser