Canonical Allele Identifier: CA375631462

Gene: NOTCH1

Linked Data

• dbSNP Id: rs200254239
• MyVariant Identifiers: chr9:g.139391682C>G (hg19) ; chr9:g.136497230C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497230C>G , CM000671.2:g.136497230C>G	GRCh38
NC_000009.11:g.139391682C>G , CM000671.1:g.139391682C>G	GRCh37
NC_000009.10:g.138511503C>G	NCBI36
NG_007458.1:g.53557G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6509G>C MANE Select	ENSP00000498587.1:p.Ser2170Thr
ENST00000679595.1:c.*1549G>C	ENSP00000506241.1:n.*1549G>C
ENST00000679969.1:n.3105G>C
ENST00000680003.1:n.2841G>C
ENST00000680133.1:c.6395G>C	ENSP00000505319.1:p.Ser2132Thr
ENST00000680218.1:c.6389G>C	ENSP00000505339.1:p.Ser2130Thr
ENST00000680668.1:c.6395G>C	ENSP00000506336.1:p.Ser2132Thr
ENST00000680778.1:c.4106G>C	ENSP00000506033.1:p.Ser1369Thr
ENST00000680924.1:c.*3909G>C	ENSP00000506031.1:n.*3909G>C
ENST00000681135.1:c.*4118G>C	ENSP00000506636.1:n.*4118G>C
ENST00000681298.1:n.4614G>C
ENST00000681454.1:c.*5745G>C	ENSP00000505763.1:n.*5745G>C
ENST00000277541.6:c.6509G>C	ENSP00000277541.6:p.Ser2170Thr
NM_017617.3:c.6509G>C	NP_060087.3:p.Ser2170Thr
XM_011518717.1:c.5810G>C	XP_011517019.1:p.Ser1937Thr
NM_017617.5:c.6509G>C MANE Select	NP_060087.3:p.Ser2170Thr
XM_011518717.2:c.5786G>C	XP_011517019.2:p.Ser1929Thr