Canonical Allele Identifier: CA375499985

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138656926A>C (hg19) ; chr9:g.135765080A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765080A>C , CM000671.2:g.135765080A>C	GRCh38
NC_000009.11:g.138656926A>C , CM000671.1:g.138656926A>C	GRCh37
NC_000009.10:g.137796747A>C	NCBI36
NG_033070.1:g.67896A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1085A>C MANE Select	ENSP00000360822.2:p.Asn362Thr
ENST00000674572.1:c.926A>C	ENSP00000501742.1:p.Asn309Thr
ENST00000675090.1:c.833A>C	ENSP00000501833.1:p.Asn278Thr
ENST00000675399.1:c.833A>C	ENSP00000501932.1:p.Asn278Thr
ENST00000676421.1:c.842A>C	ENSP00000502322.1:p.Asn281Thr
ENST00000263604.5:c.986A>C	ENSP00000263604.4:p.Asn329Thr
ENST00000371757.6:c.1085A>C	ENSP00000360822.2:p.Asn362Thr
ENST00000460750.5:c.*695A>C	ENSP00000418777.1:n.*695A>C
ENST00000486577.6:c.968A>C	ENSP00000417578.3:p.Asn323Thr
ENST00000487664.5:c.1085A>C	ENSP00000417851.2:p.Asn362Thr
ENST00000488444.6:c.1028A>C	ENSP00000419007.3:p.Asn343Thr
ENST00000490355.6:c.1028A>C	ENSP00000418003.3:p.Asn343Thr
ENST00000490363.3:n.904A>C
ENST00000491806.6:c.1028A>C	ENSP00000419086.3:p.Asn343Thr
ENST00000628528.2:c.950A>C	ENSP00000486374.1:p.Asn317Thr
ENST00000630792.2:c.926A>C	ENSP00000486486.1:p.Asn309Thr
ENST00000631073.2:c.1028A>C	ENSP00000486130.1:p.Asn343Thr
NM_001272003.1:c.950A>C	NP_001258932.1:p.Asn317Thr
NM_020822.2:c.1085A>C	NP_065873.2:p.Asn362Thr
XM_011518877.1:c.1220A>C	XP_011517179.1:p.Asn407Thr
XM_011518878.1:c.1229A>C	XP_011517180.1:p.Asn410Thr
XM_011518879.1:c.1220A>C	XP_011517181.1:p.Asn407Thr
XM_011518880.1:c.986A>C	XP_011517182.1:p.Asn329Thr
XM_011518881.1:c.575A>C	XP_011517183.1:p.Asn192Thr
XM_011518877.3:c.1220A>C	XP_011517179.1:p.Asn407Thr
XM_011518878.3:c.1229A>C	XP_011517180.1:p.Asn410Thr
XM_011518879.3:c.1220A>C	XP_011517181.1:p.Asn407Thr
XM_011518881.3:c.575A>C	XP_011517183.1:p.Asn192Thr
XM_017014931.1:c.1019A>C	XP_016870420.1:p.Asn340Thr
XM_017014932.1:c.842A>C	XP_016870421.1:p.Asn281Thr
XM_017014933.1:c.575A>C	XP_016870422.1:p.Asn192Thr
XM_024447617.1:c.575A>C	XP_024303385.1:p.Asn192Thr
XM_024447618.1:c.575A>C	XP_024303386.1:p.Asn192Thr
NM_020822.3:c.1085A>C MANE Select	NP_065873.2:p.Asn362Thr
NM_001272003.2:c.950A>C	NP_001258932.1:p.Asn317Thr