Canonical Allele Identifier: CA375501560

Gene: KCNT1

Linked Data

• gnomAD v4: 9-135765709-T-C
• MyVariant Identifiers: chr9:g.138657555T>C (hg19) ; chr9:g.135765709T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765709T>C , CM000671.2:g.135765709T>C	GRCh38
NC_000009.11:g.138657555T>C , CM000671.1:g.138657555T>C	GRCh37
NC_000009.10:g.137797376T>C	NCBI36
NG_033070.1:g.68525T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1286T>C MANE Select	ENSP00000360822.2:p.Val429Ala
ENST00000636995.1:n.13T>C
ENST00000637798.1:n.25T>C
ENST00000674572.1:c.1127T>C	ENSP00000501742.1:p.Val376Ala
ENST00000675090.1:c.1034T>C	ENSP00000501833.1:p.Val345Ala
ENST00000675399.1:c.1034T>C	ENSP00000501932.1:p.Val345Ala
ENST00000676421.1:c.1043T>C	ENSP00000502322.1:p.Val348Ala
ENST00000263604.5:c.1187T>C	ENSP00000263604.4:p.Val396Ala
ENST00000371757.6:c.1286T>C	ENSP00000360822.2:p.Val429Ala
ENST00000460750.5:c.*896T>C	ENSP00000418777.1:n.*896T>C
ENST00000486577.6:c.1169T>C	ENSP00000417578.3:p.Val390Ala
ENST00000487664.5:c.1286T>C	ENSP00000417851.2:p.Val429Ala
ENST00000488444.6:c.1229T>C	ENSP00000419007.3:p.Val410Ala
ENST00000490355.6:c.1229T>C	ENSP00000418003.3:p.Val410Ala
ENST00000490363.3:n.1105T>C
ENST00000491806.6:c.1229T>C	ENSP00000419086.3:p.Val410Ala
ENST00000628528.2:c.1151T>C	ENSP00000486374.1:p.Val384Ala
ENST00000630792.2:c.1127T>C	ENSP00000486486.1:p.Val376Ala
ENST00000631073.2:c.1229T>C	ENSP00000486130.1:p.Val410Ala
NM_001272003.1:c.1151T>C	NP_001258932.1:p.Val384Ala
NM_020822.2:c.1286T>C	NP_065873.2:p.Val429Ala
XM_011518877.1:c.1421T>C	XP_011517179.1:p.Val474Ala
XM_011518878.1:c.1430T>C	XP_011517180.1:p.Val477Ala
XM_011518879.1:c.1421T>C	XP_011517181.1:p.Val474Ala
XM_011518880.1:c.1187T>C	XP_011517182.1:p.Val396Ala
XM_011518881.1:c.776T>C	XP_011517183.1:p.Val259Ala
XM_011518877.3:c.1421T>C	XP_011517179.1:p.Val474Ala
XM_011518878.3:c.1430T>C	XP_011517180.1:p.Val477Ala
XM_011518879.3:c.1421T>C	XP_011517181.1:p.Val474Ala
XM_011518881.3:c.776T>C	XP_011517183.1:p.Val259Ala
XM_017014931.1:c.1220T>C	XP_016870420.1:p.Val407Ala
XM_017014932.1:c.1043T>C	XP_016870421.1:p.Val348Ala
XM_017014933.1:c.776T>C	XP_016870422.1:p.Val259Ala
XM_024447617.1:c.776T>C	XP_024303385.1:p.Val259Ala
XM_024447618.1:c.776T>C	XP_024303386.1:p.Val259Ala
NM_020822.3:c.1286T>C MANE Select	NP_065873.2:p.Val429Ala
NM_001272003.2:c.1151T>C	NP_001258932.1:p.Val384Ala