Canonical Allele Identifier: CA375512140

Gene: KCNT1

Linked Data

• gnomAD v4: 9-135775321-G-T
• MyVariant Identifiers: chr9:g.138667167G>T (hg19) ; chr9:g.135775321G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135775321G>T , CM000671.2:g.135775321G>T	GRCh38
NC_000009.11:g.138667167G>T , CM000671.1:g.138667167G>T	GRCh37
NC_000009.10:g.137806988G>T	NCBI36
NG_033070.1:g.78137G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.2255G>T MANE Select	ENSP00000360822.2:p.Gly752Val
ENST00000674572.1:c.2096G>T	ENSP00000501742.1:p.Gly699Val
ENST00000675090.1:c.2003G>T	ENSP00000501833.1:p.Gly668Val
ENST00000675399.1:c.2003G>T	ENSP00000501932.1:p.Gly668Val
ENST00000676421.1:c.2012G>T	ENSP00000502322.1:p.Gly671Val
ENST00000263604.5:c.2156G>T	ENSP00000263604.4:p.Gly719Val
ENST00000371757.6:c.2255G>T	ENSP00000360822.2:p.Gly752Val
ENST00000460750.5:c.*1865G>T	ENSP00000418777.1:n.*1865G>T
ENST00000486577.6:c.2138G>T	ENSP00000417578.3:p.Gly713Val
ENST00000487664.5:c.2255G>T	ENSP00000417851.2:p.Gly752Val
ENST00000488444.6:c.2198G>T	ENSP00000419007.3:p.Gly733Val
ENST00000490355.6:c.2192G>T	ENSP00000418003.3:p.Gly731Val
ENST00000490363.3:n.2074G>T
ENST00000491806.6:c.2198G>T	ENSP00000419086.3:p.Gly733Val
ENST00000628528.2:c.2120G>T	ENSP00000486374.1:p.Gly707Val
ENST00000630792.2:c.2090G>T	ENSP00000486486.1:p.Gly697Val
ENST00000631073.2:c.2198G>T	ENSP00000486130.1:p.Gly733Val
ENST00000631193.1:c.104G>T	ENSP00000486830.1:p.Gly35Val
NM_001272003.1:c.2120G>T	NP_001258932.1:p.Gly707Val
NM_020822.2:c.2255G>T	NP_065873.2:p.Gly752Val
XM_011518877.1:c.2390G>T	XP_011517179.1:p.Gly797Val
XM_011518878.1:c.2399G>T	XP_011517180.1:p.Gly800Val
XM_011518879.1:c.2390G>T	XP_011517181.1:p.Gly797Val
XM_011518880.1:c.2156G>T	XP_011517182.1:p.Gly719Val
XM_011518881.1:c.1745G>T	XP_011517183.1:p.Gly582Val
XM_011518877.3:c.2390G>T	XP_011517179.1:p.Gly797Val
XM_011518878.3:c.2399G>T	XP_011517180.1:p.Gly800Val
XM_011518879.3:c.2390G>T	XP_011517181.1:p.Gly797Val
XM_011518881.3:c.1745G>T	XP_011517183.1:p.Gly582Val
XM_017014931.1:c.2189G>T	XP_016870420.1:p.Gly730Val
XM_017014932.1:c.2012G>T	XP_016870421.1:p.Gly671Val
XM_017014933.1:c.1745G>T	XP_016870422.1:p.Gly582Val
XM_024447617.1:c.1745G>T	XP_024303385.1:p.Gly582Val
XM_024447618.1:c.1745G>T	XP_024303386.1:p.Gly582Val
NM_020822.3:c.2255G>T MANE Select	NP_065873.2:p.Gly752Val
NM_001272003.2:c.2120G>T	NP_001258932.1:p.Gly707Val