Canonical Allele Identifier: CA2678132116

Gene: NOTCH4

Linked Data

• gnomAD v4: 6-32202695-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32202696dup , CM000668.2:g.32202696dup	GRCh38
NC_000006.11:g.32170473dup , CM000668.1:g.32170473dup	GRCh37
NC_000006.10:g.32278451dup	NCBI36
NG_028190.1:g.26372dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375023.3:c.3232-97dup MANE Select	ENSP00000364163.3:n.3232-97dup
ENST00000474612.1:n.1221dup
NM_004557.3:c.3232-97dup	NP_004548.3:n.3232-97dup
NR_134949.1:n.3472+1074dup
NR_134950.1:n.3370+1074dup
NM_004557.4:c.3232-97dup MANE Select	NP_004548.3:n.3232-97dup
NR_134949.2:n.3472+1074dup
NR_134950.2:n.3370+1074dup