Canonical Allele Identifier: CA375645751

Gene: NOTCH1

Linked Data

• dbSNP Id: rs774068657
• MyVariant Identifiers: chr9:g.139399491C>G (hg19) ; chr9:g.136505039C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136505039C>G , CM000671.2:g.136505039C>G	GRCh38
NC_000009.11:g.139399491C>G , CM000671.1:g.139399491C>G	GRCh37
NC_000009.10:g.138519312C>G	NCBI36
NG_007458.1:g.45748G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2459G>C
ENST00000651671.1:c.4652G>C MANE Select	ENSP00000498587.1:p.Ser1551Thr
ENST00000679595.1:c.4652G>C	ENSP00000506241.1:p.Ser1551Thr
ENST00000680133.1:c.4538G>C	ENSP00000505319.1:p.Ser1513Thr
ENST00000680218.1:c.4532G>C	ENSP00000505339.1:p.Ser1511Thr
ENST00000680668.1:c.4538G>C	ENSP00000506336.1:p.Ser1513Thr
ENST00000680778.1:c.2249G>C	ENSP00000506033.1:p.Ser750Thr
ENST00000680924.1:c.*2052G>C	ENSP00000506031.1:n.*2052G>C
ENST00000681135.1:c.*2261G>C	ENSP00000506636.1:n.*2261G>C
ENST00000681298.1:n.1465G>C
ENST00000681454.1:c.*3888G>C	ENSP00000505763.1:n.*3888G>C
ENST00000277541.6:c.4652G>C	ENSP00000277541.6:p.Ser1551Thr
NM_017617.3:c.4652G>C	NP_060087.3:p.Ser1551Thr
XM_011518717.1:c.3953G>C	XP_011517019.1:p.Ser1318Thr
NM_017617.5:c.4652G>C MANE Select	NP_060087.3:p.Ser1551Thr
XM_011518717.2:c.3929G>C	XP_011517019.2:p.Ser1310Thr