Canonical Allele Identifier: CA375494721

Gene: KCNT1

Linked Data

• MyVariant Identifiers: chr9:g.138641960T>C (hg19) ; chr9:g.135750114T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135750114T>C , CM000671.2:g.135750114T>C	GRCh38
NC_000009.11:g.138641960T>C , CM000671.1:g.138641960T>C	GRCh37
NC_000009.10:g.137781781T>C	NCBI36
NG_033070.1:g.52930T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371757.7:c.271T>C MANE Select	ENSP00000360822.2:p.Tyr91His
ENST00000637018.1:n.76T>C
ENST00000638123.1:n.6T>C
ENST00000674572.1:c.112T>C	ENSP00000501742.1:p.Tyr38His
ENST00000675090.1:c.19T>C	ENSP00000501833.1:p.Tyr7His
ENST00000675399.1:c.19T>C	ENSP00000501932.1:p.Tyr7His
ENST00000676421.1:c.19T>C	ENSP00000502322.1:p.Tyr7His
ENST00000263604.5:c.172T>C	ENSP00000263604.4:p.Tyr58His
ENST00000371757.6:c.271T>C	ENSP00000360822.2:p.Tyr91His
ENST00000460750.5:c.271T>C	ENSP00000418777.1:p.Tyr91His
ENST00000473941.5:c.112T>C	ENSP00000420764.1:p.Tyr38His
ENST00000486577.6:c.154T>C	ENSP00000417578.3:p.Tyr52His
ENST00000487664.5:c.271T>C	ENSP00000417851.2:p.Tyr91His
ENST00000488444.6:c.214T>C	ENSP00000419007.3:p.Tyr72His
ENST00000490355.6:c.214T>C	ENSP00000418003.3:p.Tyr72His
ENST00000491806.6:c.214T>C	ENSP00000419086.3:p.Tyr72His
ENST00000628528.2:c.127T>C	ENSP00000486374.1:p.Tyr43His
ENST00000630792.2:c.112T>C	ENSP00000486486.1:p.Tyr38His
ENST00000631073.2:c.214T>C	ENSP00000486130.1:p.Tyr72His
NM_001272003.1:c.127T>C	NP_001258932.1:p.Tyr43His
NM_020822.2:c.271T>C	NP_065873.2:p.Tyr91His
XM_011518877.1:c.406T>C	XP_011517179.1:p.Tyr136His
XM_011518878.1:c.406T>C	XP_011517180.1:p.Tyr136His
XM_011518879.1:c.406T>C	XP_011517181.1:p.Tyr136His
XM_011518880.1:c.172T>C	XP_011517182.1:p.Tyr58His
XM_011518877.3:c.406T>C	XP_011517179.1:p.Tyr136His
XM_011518878.3:c.406T>C	XP_011517180.1:p.Tyr136His
XM_011518879.3:c.406T>C	XP_011517181.1:p.Tyr136His
XM_017014931.1:c.296T>C	XP_016870420.1:p.Leu99Pro
XM_017014932.1:c.19T>C	XP_016870421.1:p.Tyr7His
XM_017014933.1:c.-149T>C	XP_016870422.1:n.-149T>C
XM_024447617.1:c.-249T>C	XP_024303385.1:n.-249T>C
XM_024447618.1:c.-249T>C	XP_024303386.1:n.-249T>C
NM_020822.3:c.271T>C MANE Select	NP_065873.2:p.Tyr91His
NM_001272003.2:c.127T>C	NP_001258932.1:p.Tyr43His