Canonical Allele Identifier: CA1619467743
Gene: NOTCH4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202691G= , CM000668.2:g.32202691G= GRCh38
NC_000006.11:g.32170468G= , CM000668.1:g.32170468G= GRCh37
NC_000006.10:g.32278446G= NCBI36
NG_028190.1:g.26377C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-92C= MANE Select ENSP00000364163.3:n.3232-92C=
ENST00000474612.1:n.1226C=
NM_004557.3:c.3232-92C= NP_004548.3:n.3232-92C=
NR_134949.1:n.3472+1079C=
NR_134950.1:n.3370+1079C=
NM_004557.4:c.3232-92C= MANE Select NP_004548.3:n.3232-92C=
NR_134949.2:n.3472+1079C=
NR_134950.2:n.3370+1079C=
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