Canonical Allele Identifier: CA363557590
Gene: NOTCH4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32220821T>C , CM000668.2:g.32220821T>C GRCh38
NC_000006.11:g.32188598T>C , CM000668.1:g.32188598T>C GRCh37
NC_000006.10:g.32296576T>C NCBI36
NG_028190.1:g.8247A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.857A>G MANE Select ENSP00000364163.3:p.Gln286Arg
ENST00000473562.1:n.986A>G
NM_004557.3:c.857A>G NP_004548.3:p.Gln286Arg
NR_134949.1:n.996A>G
NR_134950.1:n.996A>G
NM_004557.4:c.857A>G MANE Select NP_004548.3:p.Gln286Arg
NR_134949.2:n.996A>G
NR_134950.2:n.996A>G