Canonical Allele Identifier: CA375493912

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138683685T>G (hg19) ; chr9:g.135791839T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135791839T>G , CM000671.2:g.135791839T>G	GRCh38
NC_000009.11:g.138683685T>G , CM000671.1:g.138683685T>G	GRCh37
NC_000009.10:g.137823506T>G	NCBI36
NG_033070.1:g.94655T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.3545T>G MANE Select	ENSP00000360822.2:p.Ile1182Ser
ENST00000674572.1:c.3449T>G	ENSP00000501742.1:p.Ile1150Ser
ENST00000675090.1:c.3293T>G	ENSP00000501833.1:p.Ile1098Ser
ENST00000675399.1:c.3356T>G	ENSP00000501932.1:p.Ile1119Ser
ENST00000676421.1:c.3365T>G	ENSP00000502322.1:p.Ile1122Ser
ENST00000263604.5:c.3509T>G	ENSP00000263604.4:p.Ile1170Ser
ENST00000371757.6:c.3545T>G	ENSP00000360822.2:p.Ile1182Ser
ENST00000460750.5:c.*3218T>G	ENSP00000418777.1:n.*3218T>G
ENST00000475008.1:n.2851T>G
ENST00000486577.6:c.3491T>G	ENSP00000417578.3:p.Ile1164Ser
ENST00000487664.5:c.3608T>G	ENSP00000417851.2:p.Ile1203Ser
ENST00000488444.6:c.3530T>G	ENSP00000419007.3:p.Ile1177Ser
ENST00000490355.6:c.3545T>G	ENSP00000418003.3:p.Ile1182Ser
ENST00000491806.6:c.3488T>G	ENSP00000419086.3:p.Ile1163Ser
ENST00000628528.2:c.3473T>G	ENSP00000486374.1:p.Ile1158Ser
ENST00000630792.2:c.3443T>G	ENSP00000486486.1:p.Ile1148Ser
ENST00000631073.2:c.3551T>G	ENSP00000486130.1:p.Ile1184Ser
NM_001272003.1:c.3473T>G	NP_001258932.1:p.Ile1158Ser
NM_020822.2:c.3545T>G	NP_065873.2:p.Ile1182Ser
XM_011518877.1:c.3743T>G	XP_011517179.1:p.Ile1248Ser
XM_011518878.1:c.3689T>G	XP_011517180.1:p.Ile1230Ser
XM_011518879.1:c.3680T>G	XP_011517181.1:p.Ile1227Ser
XM_011518880.1:c.3509T>G	XP_011517182.1:p.Ile1170Ser
XM_011518881.1:c.3098T>G	XP_011517183.1:p.Ile1033Ser
XM_011518877.3:c.3743T>G	XP_011517179.1:p.Ile1248Ser
XM_011518878.3:c.3689T>G	XP_011517180.1:p.Ile1230Ser
XM_011518879.3:c.3680T>G	XP_011517181.1:p.Ile1227Ser
XM_011518881.3:c.3098T>G	XP_011517183.1:p.Ile1033Ser
XM_017014931.1:c.3542T>G	XP_016870420.1:p.Ile1181Ser
XM_017014932.1:c.3365T>G	XP_016870421.1:p.Ile1122Ser
XM_017014933.1:c.3098T>G	XP_016870422.1:p.Ile1033Ser
XM_024447617.1:c.3098T>G	XP_024303385.1:p.Ile1033Ser
XM_024447618.1:c.3098T>G	XP_024303386.1:p.Ile1033Ser
NM_020822.3:c.3545T>G MANE Select	NP_065873.2:p.Ile1182Ser
NM_001272003.2:c.3473T>G	NP_001258932.1:p.Ile1158Ser