Canonical Allele Identifier: CA1619473598
Gene: NOTCH4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32222684G= , CM000668.2:g.32222684G= GRCh38
NC_000006.11:g.32190461G= , CM000668.1:g.32190461G= GRCh37
NC_000006.10:g.32298439G= NCBI36
NG_028190.1:g.6384C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.278C= MANE Select ENSP00000364163.3:p.Ser93=
ENST00000473562.1:n.407C=
NM_004557.3:c.278C= NP_004548.3:p.Ser93=
NR_134949.1:n.417C=
NR_134950.1:n.417C=
NM_004557.4:c.278C= MANE Select NP_004548.3:p.Ser93=
NR_134949.2:n.417C=
NR_134950.2:n.417C=
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