Canonical Allele Identifier: CA1883866300

Gene: KCNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765072_135765073delinsAG , CM000671.2:g.135765072_135765073delinsAG	GRCh38
NC_000009.11:g.138656918_138656919delinsAG , CM000671.1:g.138656918_138656919delinsAG	GRCh37
NC_000009.10:g.137796739_137796740delinsAG	NCBI36
NG_033070.1:g.67888_67889delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000371757.7:c.1077_1078delinsAG MANE Select	ENSP00000360822.2:p.Ser359=
ENST00000674572.1:c.918_919delinsAG	ENSP00000501742.1:p.Ser306=
ENST00000675090.1:c.825_826delinsAG	ENSP00000501833.1:p.Ser275=
ENST00000675399.1:c.825_826delinsAG	ENSP00000501932.1:p.Ser275=
ENST00000676421.1:c.834_835delinsAG	ENSP00000502322.1:p.Ser278=
ENST00000263604.5:c.978_979delinsAG	ENSP00000263604.4:p.Ser326=
ENST00000371757.6:c.1077_1078delinsAG	ENSP00000360822.2:p.Ser359=
ENST00000460750.5:c.*687_*688delinsAG	ENSP00000418777.1:n.*687_*688delinsAG
ENST00000486577.6:c.960_961delinsAG	ENSP00000417578.3:p.Ser320=
ENST00000487664.5:c.1077_1078delinsAG	ENSP00000417851.2:p.Ser359=
ENST00000488444.6:c.1020_1021delinsAG	ENSP00000419007.3:p.Ser340=
ENST00000490355.6:c.1020_1021delinsAG	ENSP00000418003.3:p.Ser340=
ENST00000490363.3:n.896_897delinsAG
ENST00000491806.6:c.1020_1021delinsAG	ENSP00000419086.3:p.Ser340=
ENST00000628528.2:c.942_943delinsAG	ENSP00000486374.1:p.Ser314=
ENST00000630792.2:c.918_919delinsAG	ENSP00000486486.1:p.Ser306=
ENST00000631073.2:c.1020_1021delinsAG	ENSP00000486130.1:p.Ser340=
NM_001272003.1:c.942_943delinsAG	NP_001258932.1:p.Ser314=
NM_020822.2:c.1077_1078delinsAG	NP_065873.2:p.Ser359=
XM_011518877.1:c.1212_1213delinsAG	XP_011517179.1:p.Ser404=
XM_011518878.1:c.1221_1222delinsAG	XP_011517180.1:p.Ser407=
XM_011518879.1:c.1212_1213delinsAG	XP_011517181.1:p.Ser404=
XM_011518880.1:c.978_979delinsAG	XP_011517182.1:p.Ser326=
XM_011518881.1:c.567_568delinsAG	XP_011517183.1:p.Ser189=
XM_011518877.3:c.1212_1213delinsAG	XP_011517179.1:p.Ser404=
XM_011518878.3:c.1221_1222delinsAG	XP_011517180.1:p.Ser407=
XM_011518879.3:c.1212_1213delinsAG	XP_011517181.1:p.Ser404=
XM_011518881.3:c.567_568delinsAG	XP_011517183.1:p.Ser189=
XM_017014931.1:c.1011_1012delinsAG	XP_016870420.1:p.Ser337=
XM_017014932.1:c.834_835delinsAG	XP_016870421.1:p.Ser278=
XM_017014933.1:c.567_568delinsAG	XP_016870422.1:p.Ser189=
XM_024447617.1:c.567_568delinsAG	XP_024303385.1:p.Ser189=
XM_024447618.1:c.567_568delinsAG	XP_024303386.1:p.Ser189=
NM_020822.3:c.1077_1078delinsAG MANE Select	NP_065873.2:p.Ser359=
NM_001272003.2:c.942_943delinsAG	NP_001258932.1:p.Ser314=