Canonical Allele Identifier: CA1619467812
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202927_32202929delinsCAG , CM000668.2:g.32202927_32202929delinsCAG GRCh38
NC_000006.11:g.32170704_32170706delinsCAG , CM000668.1:g.32170704_32170706delinsCAG GRCh37
NC_000006.10:g.32278682_32278684delinsCAG NCBI36
NG_028190.1:g.26139_26141delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-330_3232-328delinsCTG MANE Select ENSP00000364163.3:n.3232-330_3232-328delinsCTG
ENST00000474612.1:n.988_990delinsCTG
NM_004557.3:c.3232-330_3232-328delinsCTG NP_004548.3:n.3232-330_3232-328delinsCTG
NR_134949.1:n.3472+841_3472+843delinsCTG
NR_134950.1:n.3370+841_3370+843delinsCTG
NM_004557.4:c.3232-330_3232-328delinsCTG MANE Select NP_004548.3:n.3232-330_3232-328delinsCTG
NR_134949.2:n.3472+841_3472+843delinsCTG
NR_134950.2:n.3370+841_3370+843delinsCTG