Canonical Allele Identifier: CA1619467814
Gene: NOTCH4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202930A= , CM000668.2:g.32202930A= GRCh38
NC_000006.11:g.32170707A= , CM000668.1:g.32170707A= GRCh37
NC_000006.10:g.32278685A= NCBI36
NG_028190.1:g.26138T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-331T= MANE Select ENSP00000364163.3:n.3232-331T=
ENST00000474612.1:n.987T=
NM_004557.3:c.3232-331T= NP_004548.3:n.3232-331T=
NR_134949.1:n.3472+840T=
NR_134950.1:n.3370+840T=
NM_004557.4:c.3232-331T= MANE Select NP_004548.3:n.3232-331T=
NR_134949.2:n.3472+840T=
NR_134950.2:n.3370+840T=
Search 100 bp 5'
Search 100 bp 3'