Canonical Allele Identifier: CA1619467722
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202659C= , CM000668.2:g.32202659C= GRCh38
NC_000006.11:g.32170436C= , CM000668.1:g.32170436C= GRCh37
NC_000006.10:g.32278414C= NCBI36
NG_028190.1:g.26409G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375023.3:c.3232-60G= MANE Select ENSP00000364163.3:n.3232-60G=
ENST00000474612.1:n.1258G=
NM_004557.3:c.3232-60G= NP_004548.3:n.3232-60G=
NR_134949.1:n.3472+1111G=
NR_134950.1:n.3370+1111G=
NM_004557.4:c.3232-60G= MANE Select NP_004548.3:n.3232-60G=
NR_134949.2:n.3472+1111G=
NR_134950.2:n.3370+1111G=