Canonical Allele Identifier: CA375501323

Gene: KCNT1

Linked Data

• gnomAD v4: 9-135765669-G-A
• COSMIC: COSM6385977 ; COSM6385978
• MyVariant Identifiers: chr9:g.138657515G>A (hg19) ; chr9:g.135765669G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135765669G>A , CM000671.2:g.135765669G>A	GRCh38
NC_000009.11:g.138657515G>A , CM000671.1:g.138657515G>A	GRCh37
NC_000009.10:g.137797336G>A	NCBI36
NG_033070.1:g.68485G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.1246G>A MANE Select	ENSP00000360822.2:p.Val416Met
ENST00000674572.1:c.1087G>A	ENSP00000501742.1:p.Val363Met
ENST00000675090.1:c.994G>A	ENSP00000501833.1:p.Val332Met
ENST00000675399.1:c.994G>A	ENSP00000501932.1:p.Val332Met
ENST00000676421.1:c.1003G>A	ENSP00000502322.1:p.Val335Met
ENST00000263604.5:c.1147G>A	ENSP00000263604.4:p.Val383Met
ENST00000371757.6:c.1246G>A	ENSP00000360822.2:p.Val416Met
ENST00000460750.5:c.*856G>A	ENSP00000418777.1:n.*856G>A
ENST00000486577.6:c.1129G>A	ENSP00000417578.3:p.Val377Met
ENST00000487664.5:c.1246G>A	ENSP00000417851.2:p.Val416Met
ENST00000488444.6:c.1189G>A	ENSP00000419007.3:p.Val397Met
ENST00000490355.6:c.1189G>A	ENSP00000418003.3:p.Val397Met
ENST00000490363.3:n.1065G>A
ENST00000491806.6:c.1189G>A	ENSP00000419086.3:p.Val397Met
ENST00000628528.2:c.1111G>A	ENSP00000486374.1:p.Val371Met
ENST00000630792.2:c.1087G>A	ENSP00000486486.1:p.Val363Met
ENST00000631073.2:c.1189G>A	ENSP00000486130.1:p.Val397Met
NM_001272003.1:c.1111G>A	NP_001258932.1:p.Val371Met
NM_020822.2:c.1246G>A	NP_065873.2:p.Val416Met
XM_011518877.1:c.1381G>A	XP_011517179.1:p.Val461Met
XM_011518878.1:c.1390G>A	XP_011517180.1:p.Val464Met
XM_011518879.1:c.1381G>A	XP_011517181.1:p.Val461Met
XM_011518880.1:c.1147G>A	XP_011517182.1:p.Val383Met
XM_011518881.1:c.736G>A	XP_011517183.1:p.Val246Met
XM_011518877.3:c.1381G>A	XP_011517179.1:p.Val461Met
XM_011518878.3:c.1390G>A	XP_011517180.1:p.Val464Met
XM_011518879.3:c.1381G>A	XP_011517181.1:p.Val461Met
XM_011518881.3:c.736G>A	XP_011517183.1:p.Val246Met
XM_017014931.1:c.1180G>A	XP_016870420.1:p.Val394Met
XM_017014932.1:c.1003G>A	XP_016870421.1:p.Val335Met
XM_017014933.1:c.736G>A	XP_016870422.1:p.Val246Met
XM_024447617.1:c.736G>A	XP_024303385.1:p.Val246Met
XM_024447618.1:c.736G>A	XP_024303386.1:p.Val246Met
NM_020822.3:c.1246G>A MANE Select	NP_065873.2:p.Val416Met
NM_001272003.2:c.1111G>A	NP_001258932.1:p.Val371Met