Canonical Allele Identifier: CA375634128

Gene: NOTCH1

Linked Data

• dbSNP Id: rs1162986139
• MyVariant Identifiers: chr9:g.139393442G>T (hg19) ; chr9:g.136498990G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136498990G>T , CM000671.2:g.136498990G>T	GRCh38
NC_000009.11:g.139393442G>T , CM000671.1:g.139393442G>T	GRCh37
NC_000009.10:g.138513263G>T	NCBI36
NG_007458.1:g.51797C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6089C>A MANE Select	ENSP00000498587.1:p.Ser2030Tyr
ENST00000679595.1:c.*1129C>A	ENSP00000506241.1:n.*1129C>A
ENST00000679969.1:n.2685C>A
ENST00000680003.1:n.2421C>A
ENST00000680133.1:c.5975C>A	ENSP00000505319.1:p.Ser1992Tyr
ENST00000680218.1:c.5969C>A	ENSP00000505339.1:p.Ser1990Tyr
ENST00000680668.1:c.5975C>A	ENSP00000506336.1:p.Ser1992Tyr
ENST00000680778.1:c.3686C>A	ENSP00000506033.1:p.Ser1229Tyr
ENST00000680924.1:c.*3489C>A	ENSP00000506031.1:n.*3489C>A
ENST00000681135.1:c.*3698C>A	ENSP00000506636.1:n.*3698C>A
ENST00000681298.1:n.4194C>A
ENST00000681454.1:c.*5325C>A	ENSP00000505763.1:n.*5325C>A
ENST00000277541.6:c.6089C>A	ENSP00000277541.6:p.Ser2030Tyr
NM_017617.3:c.6089C>A	NP_060087.3:p.Ser2030Tyr
XM_011518717.1:c.5390C>A	XP_011517019.1:p.Ser1797Tyr
NM_017617.5:c.6089C>A MANE Select	NP_060087.3:p.Ser2030Tyr
XM_011518717.2:c.5366C>A	XP_011517019.2:p.Ser1789Tyr