Canonical Allele Identifier: CA1619467805
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202902A= , CM000668.2:g.32202902A= GRCh38
NC_000006.11:g.32170679A= , CM000668.1:g.32170679A= GRCh37
NC_000006.10:g.32278657A= NCBI36
NG_028190.1:g.26166T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-303T= MANE Select ENSP00000364163.3:n.3232-303T=
ENST00000474612.1:n.1015T=
NM_004557.3:c.3232-303T= NP_004548.3:n.3232-303T=
NR_134949.1:n.3472+868T=
NR_134950.1:n.3370+868T=
NM_004557.4:c.3232-303T= MANE Select NP_004548.3:n.3232-303T=
NR_134949.2:n.3472+868T=
NR_134950.2:n.3370+868T=