Canonical Allele Identifier: CA2692634842
Gene: NOTCH1 HGNC NCBI

Linked Data

dbSNP Id: rs773097159

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136505128G>C , CM000671.2:g.136505128G>C GRCh38
NC_000009.11:g.139399580G>C , CM000671.1:g.139399580G>C GRCh37
NC_000009.10:g.138519401G>C NCBI36
NG_007458.1:g.45659C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645828.1:n.2394-24C>G
ENST00000651671.1:c.4587-24C>G MANE Select ENSP00000498587.1:n.4587-24C>G
ENST00000679595.1:c.4587-24C>G ENSP00000506241.1:n.4587-24C>G
ENST00000680133.1:c.4473-24C>G ENSP00000505319.1:n.4473-24C>G
ENST00000680218.1:c.4467-24C>G ENSP00000505339.1:n.4467-24C>G
ENST00000680668.1:c.4473-24C>G ENSP00000506336.1:n.4473-24C>G
ENST00000680778.1:c.2184-24C>G ENSP00000506033.1:n.2184-24C>G
ENST00000680924.1:c.*1987-24C>G ENSP00000506031.1:n.*1987-24C>G
ENST00000681135.1:c.*2196-24C>G ENSP00000506636.1:n.*2196-24C>G
ENST00000681298.1:n.1400-24C>G
ENST00000681454.1:c.*3823-24C>G ENSP00000505763.1:n.*3823-24C>G
ENST00000277541.6:c.4587-24C>G ENSP00000277541.6:n.4587-24C>G
NM_017617.3:c.4587-24C>G NP_060087.3:n.4587-24C>G
XM_011518717.1:c.3888-24C>G XP_011517019.1:n.3888-24C>G
NM_017617.5:c.4587-24C>G MANE Select NP_060087.3:n.4587-24C>G
XM_011518717.2:c.3864-24C>G XP_011517019.2:n.3864-24C>G