Canonical Allele Identifier: CA2560619921
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202856A>G , CM000668.2:g.32202856A>G GRCh38
NC_000006.11:g.32170633A>G , CM000668.1:g.32170633A>G GRCh37
NC_000006.10:g.32278611A>G NCBI36
NG_028190.1:g.26212T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-257T>C MANE Select ENSP00000364163.3:n.3232-257T>C
ENST00000474612.1:n.1061T>C
NM_004557.3:c.3232-257T>C NP_004548.3:n.3232-257T>C
NR_134949.1:n.3472+914T>C
NR_134950.1:n.3370+914T>C
NM_004557.4:c.3232-257T>C MANE Select NP_004548.3:n.3232-257T>C
NR_134949.2:n.3472+914T>C
NR_134950.2:n.3370+914T>C