Canonical Allele Identifier: CA467832736

Gene: NOTCH1

Linked Data

• dbSNP Id: rs761609069
• gnomAD v4: 9-136504891-C-A
• MyVariant Identifiers: chr9:g.139399343C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504891C>A , CM000671.2:g.136504891C>A	GRCh38
NC_000009.11:g.139399343C>A , CM000671.1:g.139399343C>A	GRCh37
NC_000009.10:g.138519164C>A	NCBI36
NG_007458.1:g.45896G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2607G>T
ENST00000651671.1:c.4800G>T MANE Select	ENSP00000498587.1:p.Leu1600=
ENST00000679595.1:c.4800G>T	ENSP00000506241.1:p.Leu1600=
ENST00000680133.1:c.4686G>T	ENSP00000505319.1:p.Leu1562=
ENST00000680218.1:c.4680G>T	ENSP00000505339.1:p.Leu1560=
ENST00000680668.1:c.4686G>T	ENSP00000506336.1:p.Leu1562=
ENST00000680778.1:c.2397G>T	ENSP00000506033.1:p.Leu799=
ENST00000680924.1:c.*2200G>T	ENSP00000506031.1:n.*2200G>T
ENST00000681135.1:c.*2409G>T	ENSP00000506636.1:n.*2409G>T
ENST00000681298.1:n.1613G>T
ENST00000681454.1:c.*4036G>T	ENSP00000505763.1:n.*4036G>T
ENST00000277541.6:c.4800G>T	ENSP00000277541.6:p.Leu1600=
NM_017617.3:c.4800G>T	NP_060087.3:p.Leu1600=
XM_011518717.1:c.4101G>T	XP_011517019.1:p.Leu1367=
NM_017617.5:c.4800G>T MANE Select	NP_060087.3:p.Leu1600=
XM_011518717.2:c.4077G>T	XP_011517019.2:p.Leu1359=