Canonical Allele Identifier: CA5326291

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135714612C>G , CM000671.2:g.135714612C>G	GRCh38
NC_000009.11:g.138606458C>G , CM000671.1:g.138606458C>G	GRCh37
NC_000009.10:g.137746279C>G	NCBI36
NG_033070.1:g.17428C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.146C>G MANE Select	ENSP00000360822.2:p.Thr49Ser
ENST00000674572.1:c.-14C>G	ENSP00000501742.1:n.-14C>G
ENST00000371757.6:c.146C>G	ENSP00000360822.2:p.Thr49Ser
ENST00000460750.5:c.146C>G	ENSP00000418777.1:p.Thr49Ser
ENST00000473941.5:c.-14C>G	ENSP00000420764.1:n.-14C>G
ENST00000486577.6:c.-14C>G	ENSP00000417578.3:n.-14C>G
ENST00000487664.5:c.146C>G	ENSP00000417851.2:p.Thr49Ser
ENST00000628528.2:c.110+12244C>G	ENSP00000486374.1:n.110+12244C>G
NM_001272003.1:c.110+12244C>G	NP_001258932.1:n.110+12244C>G
NM_020822.2:c.146C>G	NP_065873.2:p.Thr49Ser
XM_011518877.1:c.281C>G	XP_011517179.1:p.Thr94Ser
XM_011518878.1:c.281C>G	XP_011517180.1:p.Thr94Ser
XM_011518879.1:c.281C>G	XP_011517181.1:p.Thr94Ser
XM_011518877.3:c.281C>G	XP_011517179.1:p.Thr94Ser
XM_011518878.3:c.281C>G	XP_011517180.1:p.Thr94Ser
XM_011518879.3:c.281C>G	XP_011517181.1:p.Thr94Ser
NM_020822.3:c.146C>G MANE Select	NP_065873.2:p.Thr49Ser
NM_001272003.2:c.110+12244C>G	NP_001258932.1:n.110+12244C>G