Canonical Allele Identifier: CA1883892364
Gene: KCNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135791650G= , CM000671.2:g.135791650G= GRCh38
NC_000009.11:g.138683496G= , CM000671.1:g.138683496G= GRCh37
NC_000009.10:g.137823317G= NCBI36
NG_033070.1:g.94466G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371757.7:c.3503-147G= MANE Select ENSP00000360822.2:n.3503-147G=
ENST00000674572.1:c.3407-147G= ENSP00000501742.1:n.3407-147G=
ENST00000675090.1:c.3251-147G= ENSP00000501833.1:n.3251-147G=
ENST00000675399.1:c.3314-147G= ENSP00000501932.1:n.3314-147G=
ENST00000676421.1:c.3323-147G= ENSP00000502322.1:n.3323-147G=
ENST00000263604.5:c.3467-147G= ENSP00000263604.4:n.3467-147G=
ENST00000371757.6:c.3503-147G= ENSP00000360822.2:n.3503-147G=
ENST00000460750.5:c.*3176-147G= ENSP00000418777.1:n.*3176-147G=
ENST00000475008.1:n.2662G=
ENST00000486577.6:c.3449-147G= ENSP00000417578.3:n.3449-147G=
ENST00000487664.5:c.3566-147G= ENSP00000417851.2:n.3566-147G=
ENST00000488444.6:c.3488-147G= ENSP00000419007.3:n.3488-147G=
ENST00000490355.6:c.3503-147G= ENSP00000418003.3:n.3503-147G=
ENST00000491806.6:c.3446-147G= ENSP00000419086.3:n.3446-147G=
ENST00000628528.2:c.3431-147G= ENSP00000486374.1:n.3431-147G=
ENST00000630792.2:c.3401-147G= ENSP00000486486.1:n.3401-147G=
ENST00000631073.2:c.3509-147G= ENSP00000486130.1:n.3509-147G=
NM_001272003.1:c.3431-147G= NP_001258932.1:n.3431-147G=
NM_020822.2:c.3503-147G= NP_065873.2:n.3503-147G=
XM_011518877.1:c.3701-147G= XP_011517179.1:n.3701-147G=
XM_011518878.1:c.3647-147G= XP_011517180.1:n.3647-147G=
XM_011518879.1:c.3638-147G= XP_011517181.1:n.3638-147G=
XM_011518880.1:c.3467-147G= XP_011517182.1:n.3467-147G=
XM_011518881.1:c.3056-147G= XP_011517183.1:n.3056-147G=
XM_011518877.3:c.3701-147G= XP_011517179.1:n.3701-147G=
XM_011518878.3:c.3647-147G= XP_011517180.1:n.3647-147G=
XM_011518879.3:c.3638-147G= XP_011517181.1:n.3638-147G=
XM_011518881.3:c.3056-147G= XP_011517183.1:n.3056-147G=
XM_017014931.1:c.3500-147G= XP_016870420.1:n.3500-147G=
XM_017014932.1:c.3323-147G= XP_016870421.1:n.3323-147G=
XM_017014933.1:c.3056-147G= XP_016870422.1:n.3056-147G=
XM_024447617.1:c.3056-147G= XP_024303385.1:n.3056-147G=
XM_024447618.1:c.3056-147G= XP_024303386.1:n.3056-147G=
XR_001746978.1:n.140C=
NM_020822.3:c.3503-147G= MANE Select NP_065873.2:n.3503-147G=
NM_001272003.2:c.3431-147G= NP_001258932.1:n.3431-147G=