Canonical Allele Identifier: CA3165530954
Community Standard Title: NM_017617.5(NOTCH1):c.743-1G=
Gene: NOTCH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136519566C= , CM000671.2:g.136519566C= GRCh38
NC_000009.11:g.139414018C= , CM000671.1:g.139414018C= GRCh37
NC_000009.10:g.138533839C= NCBI36
NG_007458.1:g.31221G=

Transcript Alleles

HGVS Amino-acid Change
NM_017617.5:c.743-1G= MANE Select NP_060087.3:n.743-1G=
ENST00000651671.1:c.743-1G= MANE Select ENSP00000498587.1:n.743-1G=
NM_017617.3:c.743-1G= NP_060087.3:n.743-1G=
ENST00000277541.6:c.743-1G= ENSP00000277541.6:n.743-1G=
ENST00000679595.1:c.743-1G= ENSP00000506241.1:n.743-1G=
ENST00000680133.1:c.743-1G= ENSP00000505319.1:n.743-1G=
ENST00000680218.1:c.743-1G= ENSP00000505339.1:n.743-1G=
ENST00000680668.1:c.743-1G= ENSP00000506336.1:n.743-1G=
ENST00000680924.1:c.743-1G= ENSP00000506031.1:n.743-1G=
ENST00000681135.1:c.743-1G= ENSP00000506636.1:n.743-1G=
ENST00000681454.1:c.141-1G= ENSP00000505763.1:n.141-1G=
XM_011518717.1:c.44-1G= XP_011517019.1:n.44-1G=
XM_011518717.2:c.20-1G= XP_011517019.2:n.20-1G=