Canonical Allele Identifier: CA860977005

Gene: KCNT1

Linked Data

• dbSNP Id: rs1164610769
• gnomAD v3: 9-135791697-A-G
• gnomAD v4: 9-135791697-A-G
• MyVariant Identifiers: chr9:g.138683543A>G (hg19) ; chr9:g.135791697A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135791697A>G , CM000671.2:g.135791697A>G	GRCh38
NC_000009.11:g.138683543A>G , CM000671.1:g.138683543A>G	GRCh37
NC_000009.10:g.137823364A>G	NCBI36
NG_033070.1:g.94513A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.3503-100A>G MANE Select	ENSP00000360822.2:n.3503-100A>G
ENST00000674572.1:c.3407-100A>G	ENSP00000501742.1:n.3407-100A>G
ENST00000675090.1:c.3251-100A>G	ENSP00000501833.1:n.3251-100A>G
ENST00000675399.1:c.3314-100A>G	ENSP00000501932.1:n.3314-100A>G
ENST00000676421.1:c.3323-100A>G	ENSP00000502322.1:n.3323-100A>G
ENST00000263604.5:c.3467-100A>G	ENSP00000263604.4:n.3467-100A>G
ENST00000371757.6:c.3503-100A>G	ENSP00000360822.2:n.3503-100A>G
ENST00000460750.5:c.*3176-100A>G	ENSP00000418777.1:n.*3176-100A>G
ENST00000475008.1:n.2709A>G
ENST00000486577.6:c.3449-100A>G	ENSP00000417578.3:n.3449-100A>G
ENST00000487664.5:c.3566-100A>G	ENSP00000417851.2:n.3566-100A>G
ENST00000488444.6:c.3488-100A>G	ENSP00000419007.3:n.3488-100A>G
ENST00000490355.6:c.3503-100A>G	ENSP00000418003.3:n.3503-100A>G
ENST00000491806.6:c.3446-100A>G	ENSP00000419086.3:n.3446-100A>G
ENST00000628528.2:c.3431-100A>G	ENSP00000486374.1:n.3431-100A>G
ENST00000630792.2:c.3401-100A>G	ENSP00000486486.1:n.3401-100A>G
ENST00000631073.2:c.3509-100A>G	ENSP00000486130.1:n.3509-100A>G
NM_001272003.1:c.3431-100A>G	NP_001258932.1:n.3431-100A>G
NM_020822.2:c.3503-100A>G	NP_065873.2:n.3503-100A>G
XM_011518877.1:c.3701-100A>G	XP_011517179.1:n.3701-100A>G
XM_011518878.1:c.3647-100A>G	XP_011517180.1:n.3647-100A>G
XM_011518879.1:c.3638-100A>G	XP_011517181.1:n.3638-100A>G
XM_011518880.1:c.3467-100A>G	XP_011517182.1:n.3467-100A>G
XM_011518881.1:c.3056-100A>G	XP_011517183.1:n.3056-100A>G
XM_011518877.3:c.3701-100A>G	XP_011517179.1:n.3701-100A>G
XM_011518878.3:c.3647-100A>G	XP_011517180.1:n.3647-100A>G
XM_011518879.3:c.3638-100A>G	XP_011517181.1:n.3638-100A>G
XM_011518881.3:c.3056-100A>G	XP_011517183.1:n.3056-100A>G
XM_017014931.1:c.3500-100A>G	XP_016870420.1:n.3500-100A>G
XM_017014932.1:c.3323-100A>G	XP_016870421.1:n.3323-100A>G
XM_017014933.1:c.3056-100A>G	XP_016870422.1:n.3056-100A>G
XM_024447617.1:c.3056-100A>G	XP_024303385.1:n.3056-100A>G
XM_024447618.1:c.3056-100A>G	XP_024303386.1:n.3056-100A>G
XR_001746978.1:n.93T>C
NM_020822.3:c.3503-100A>G MANE Select	NP_065873.2:n.3503-100A>G
NM_001272003.2:c.3431-100A>G	NP_001258932.1:n.3431-100A>G