Canonical Allele Identifier: CA363557489

Gene: NOTCH4

Linked Data

• MyVariant Identifiers: chr6:g.32188553A>T (hg19) ; chr6:g.32220776A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32220776A>T , CM000668.2:g.32220776A>T	GRCh38
NC_000006.11:g.32188553A>T , CM000668.1:g.32188553A>T	GRCh37
NC_000006.10:g.32296531A>T	NCBI36
NG_028190.1:g.8292T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375023.3:c.902T>A MANE Select	ENSP00000364163.3:p.Leu301His
ENST00000473562.1:n.1031T>A
NM_004557.3:c.902T>A	NP_004548.3:p.Leu301His
NR_134949.1:n.1041T>A
NR_134950.1:n.1041T>A
NM_004557.4:c.902T>A MANE Select	NP_004548.3:p.Leu301His
NR_134949.2:n.1041T>A
NR_134950.2:n.1041T>A