Canonical Allele Identifier: CA2838960465
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202588dup , CM000668.2:g.32202588dup GRCh38
NC_000006.11:g.32170365dup , CM000668.1:g.32170365dup GRCh37
NC_000006.10:g.32278343dup NCBI36
NG_028190.1:g.26483dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3246dup MANE Select ENSP00000364163.3:p.Thr1083HisfsTer25
ENST00000474612.1:n.1332dup
NM_004557.3:c.3246dup NP_004548.3:p.Thr1083HisfsTer25
NR_134949.1:n.3473-1085dup
NR_134950.1:n.3371-1085dup
NM_004557.4:c.3246dup MANE Select NP_004548.3:p.Thr1083HisfsTer25
NR_134949.2:n.3473-1085dup
NR_134950.2:n.3371-1085dup