Canonical Allele Identifier: CA449828748

Gene: NOTCH4

Linked Data

• MyVariant Identifiers: chr6:g.32170338G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32202561G>T , CM000668.2:g.32202561G>T	GRCh38
NC_000006.11:g.32170338G>T , CM000668.1:g.32170338G>T	GRCh37
NC_000006.10:g.32278316G>T	NCBI36
NG_028190.1:g.26507C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375023.3:c.3270C>A MANE Select	ENSP00000364163.3:p.Ser1090=
ENST00000474612.1:n.1356C>A
NM_004557.3:c.3270C>A	NP_004548.3:p.Ser1090=
NR_134949.1:n.3473-1061C>A
NR_134950.1:n.3371-1061C>A
NM_004557.4:c.3270C>A MANE Select	NP_004548.3:p.Ser1090=
NR_134949.2:n.3473-1061C>A
NR_134950.2:n.3371-1061C>A