Canonical Allele Identifier: CA1619467794
Gene: NOTCH4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202883G= , CM000668.2:g.32202883G= GRCh38
NC_000006.11:g.32170660G= , CM000668.1:g.32170660G= GRCh37
NC_000006.10:g.32278638G= NCBI36
NG_028190.1:g.26185C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-284C= MANE Select ENSP00000364163.3:n.3232-284C=
ENST00000474612.1:n.1034C=
NM_004557.3:c.3232-284C= NP_004548.3:n.3232-284C=
NR_134949.1:n.3472+887C=
NR_134950.1:n.3370+887C=
NM_004557.4:c.3232-284C= MANE Select NP_004548.3:n.3232-284C=
NR_134949.2:n.3472+887C=
NR_134950.2:n.3370+887C=
Search 100 bp 5'
Search 100 bp 3'