Canonical Allele Identifier: CA467698133

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138657490G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765644G>C , CM000671.2:g.135765644G>C	GRCh38
NC_000009.11:g.138657490G>C , CM000671.1:g.138657490G>C	GRCh37
NC_000009.10:g.137797311G>C	NCBI36
NG_033070.1:g.68460G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1221G>C MANE Select	ENSP00000360822.2:p.Leu407=
ENST00000674572.1:c.1062G>C	ENSP00000501742.1:p.Leu354=
ENST00000675090.1:c.969G>C	ENSP00000501833.1:p.Leu323=
ENST00000675399.1:c.969G>C	ENSP00000501932.1:p.Leu323=
ENST00000676421.1:c.978G>C	ENSP00000502322.1:p.Leu326=
ENST00000263604.5:c.1122G>C	ENSP00000263604.4:p.Leu374=
ENST00000371757.6:c.1221G>C	ENSP00000360822.2:p.Leu407=
ENST00000460750.5:c.*831G>C	ENSP00000418777.1:n.*831G>C
ENST00000486577.6:c.1104G>C	ENSP00000417578.3:p.Leu368=
ENST00000487664.5:c.1221G>C	ENSP00000417851.2:p.Leu407=
ENST00000488444.6:c.1164G>C	ENSP00000419007.3:p.Leu388=
ENST00000490355.6:c.1164G>C	ENSP00000418003.3:p.Leu388=
ENST00000490363.3:n.1040G>C
ENST00000491806.6:c.1164G>C	ENSP00000419086.3:p.Leu388=
ENST00000628528.2:c.1086G>C	ENSP00000486374.1:p.Leu362=
ENST00000630792.2:c.1062G>C	ENSP00000486486.1:p.Leu354=
ENST00000631073.2:c.1164G>C	ENSP00000486130.1:p.Leu388=
NM_001272003.1:c.1086G>C	NP_001258932.1:p.Leu362=
NM_020822.2:c.1221G>C	NP_065873.2:p.Leu407=
XM_011518877.1:c.1356G>C	XP_011517179.1:p.Leu452=
XM_011518878.1:c.1365G>C	XP_011517180.1:p.Leu455=
XM_011518879.1:c.1356G>C	XP_011517181.1:p.Leu452=
XM_011518880.1:c.1122G>C	XP_011517182.1:p.Leu374=
XM_011518881.1:c.711G>C	XP_011517183.1:p.Leu237=
XM_011518877.3:c.1356G>C	XP_011517179.1:p.Leu452=
XM_011518878.3:c.1365G>C	XP_011517180.1:p.Leu455=
XM_011518879.3:c.1356G>C	XP_011517181.1:p.Leu452=
XM_011518881.3:c.711G>C	XP_011517183.1:p.Leu237=
XM_017014931.1:c.1155G>C	XP_016870420.1:p.Leu385=
XM_017014932.1:c.978G>C	XP_016870421.1:p.Leu326=
XM_017014933.1:c.711G>C	XP_016870422.1:p.Leu237=
XM_024447617.1:c.711G>C	XP_024303385.1:p.Leu237=
XM_024447618.1:c.711G>C	XP_024303386.1:p.Leu237=
NM_020822.3:c.1221G>C MANE Select	NP_065873.2:p.Leu407=
NM_001272003.2:c.1086G>C	NP_001258932.1:p.Leu362=