Canonical Allele Identifier: CA375506842

Gene: KCNT1

Linked Data

• gnomAD v4: 9-135770435-A-G
• MyVariant Identifiers: chr9:g.138662281A>G (hg19) ; chr9:g.135770435A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135770435A>G , CM000671.2:g.135770435A>G	GRCh38
NC_000009.11:g.138662281A>G , CM000671.1:g.138662281A>G	GRCh37
NC_000009.10:g.137802102A>G	NCBI36
NG_033070.1:g.73251A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1757A>G MANE Select	ENSP00000360822.2:p.His586Arg
ENST00000674572.1:c.1598A>G	ENSP00000501742.1:p.His533Arg
ENST00000675090.1:c.1505A>G	ENSP00000501833.1:p.His502Arg
ENST00000675399.1:c.1505A>G	ENSP00000501932.1:p.His502Arg
ENST00000676421.1:c.1514A>G	ENSP00000502322.1:p.His505Arg
ENST00000263604.5:c.1658A>G	ENSP00000263604.4:p.His553Arg
ENST00000371757.6:c.1757A>G	ENSP00000360822.2:p.His586Arg
ENST00000460750.5:c.*1367A>G	ENSP00000418777.1:n.*1367A>G
ENST00000486577.6:c.1640A>G	ENSP00000417578.3:p.His547Arg
ENST00000487664.5:c.1757A>G	ENSP00000417851.2:p.His586Arg
ENST00000488444.6:c.1700A>G	ENSP00000419007.3:p.His567Arg
ENST00000490355.6:c.1700A>G	ENSP00000418003.3:p.His567Arg
ENST00000490363.3:n.1576A>G
ENST00000491806.6:c.1700A>G	ENSP00000419086.3:p.His567Arg
ENST00000628528.2:c.1622A>G	ENSP00000486374.1:p.His541Arg
ENST00000630792.2:c.1598A>G	ENSP00000486486.1:p.His533Arg
ENST00000631073.2:c.1700A>G	ENSP00000486130.1:p.His567Arg
NM_001272003.1:c.1622A>G	NP_001258932.1:p.His541Arg
NM_020822.2:c.1757A>G	NP_065873.2:p.His586Arg
XM_011518877.1:c.1892A>G	XP_011517179.1:p.His631Arg
XM_011518878.1:c.1901A>G	XP_011517180.1:p.His634Arg
XM_011518879.1:c.1892A>G	XP_011517181.1:p.His631Arg
XM_011518880.1:c.1658A>G	XP_011517182.1:p.His553Arg
XM_011518881.1:c.1247A>G	XP_011517183.1:p.His416Arg
XM_011518877.3:c.1892A>G	XP_011517179.1:p.His631Arg
XM_011518878.3:c.1901A>G	XP_011517180.1:p.His634Arg
XM_011518879.3:c.1892A>G	XP_011517181.1:p.His631Arg
XM_011518881.3:c.1247A>G	XP_011517183.1:p.His416Arg
XM_017014931.1:c.1691A>G	XP_016870420.1:p.His564Arg
XM_017014932.1:c.1514A>G	XP_016870421.1:p.His505Arg
XM_017014933.1:c.1247A>G	XP_016870422.1:p.His416Arg
XM_024447617.1:c.1247A>G	XP_024303385.1:p.His416Arg
XM_024447618.1:c.1247A>G	XP_024303386.1:p.His416Arg
NM_020822.3:c.1757A>G MANE Select	NP_065873.2:p.His586Arg
NM_001272003.2:c.1622A>G	NP_001258932.1:p.His541Arg