Canonical Allele Identifier: CA375645698

Gene: NOTCH1

Linked Data

• dbSNP Id: rs1204612954
• MyVariant Identifiers: chr9:g.139399482C>G (hg19) ; chr9:g.136505030C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136505030C>G , CM000671.2:g.136505030C>G	GRCh38
NC_000009.11:g.139399482C>G , CM000671.1:g.139399482C>G	GRCh37
NC_000009.10:g.138519303C>G	NCBI36
NG_007458.1:g.45757G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2468G>C
ENST00000651671.1:c.4661G>C MANE Select	ENSP00000498587.1:p.Cys1554Ser
ENST00000679595.1:c.4661G>C	ENSP00000506241.1:p.Cys1554Ser
ENST00000680133.1:c.4547G>C	ENSP00000505319.1:p.Cys1516Ser
ENST00000680218.1:c.4541G>C	ENSP00000505339.1:p.Cys1514Ser
ENST00000680668.1:c.4547G>C	ENSP00000506336.1:p.Cys1516Ser
ENST00000680778.1:c.2258G>C	ENSP00000506033.1:p.Cys753Ser
ENST00000680924.1:c.*2061G>C	ENSP00000506031.1:n.*2061G>C
ENST00000681135.1:c.*2270G>C	ENSP00000506636.1:n.*2270G>C
ENST00000681298.1:n.1474G>C
ENST00000681454.1:c.*3897G>C	ENSP00000505763.1:n.*3897G>C
ENST00000277541.6:c.4661G>C	ENSP00000277541.6:p.Cys1554Ser
NM_017617.3:c.4661G>C	NP_060087.3:p.Cys1554Ser
XM_011518717.1:c.3962G>C	XP_011517019.1:p.Cys1321Ser
NM_017617.5:c.4661G>C MANE Select	NP_060087.3:p.Cys1554Ser
XM_011518717.2:c.3938G>C	XP_011517019.2:p.Cys1313Ser