Canonical Allele Identifier: CA823942688
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs1554147324
gnomAD v3: 6-32202900-A-AT
gnomAD v4: 6-32202900-A-AT
MyVariant Identifiers: chr6:g.32170677_32170678insT (hg19) chr6:g.32202900_32202901insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202901dup , CM000668.2:g.32202901dup GRCh38
NC_000006.11:g.32170678dup , CM000668.1:g.32170678dup GRCh37
NC_000006.10:g.32278656dup NCBI36
NG_028190.1:g.26167dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-302dup MANE Select ENSP00000364163.3:n.3232-302dup
ENST00000474612.1:n.1016dup
NM_004557.3:c.3232-302dup NP_004548.3:n.3232-302dup
NR_134949.1:n.3472+869dup
NR_134950.1:n.3370+869dup
NM_004557.4:c.3232-302dup MANE Select NP_004548.3:n.3232-302dup
NR_134949.2:n.3472+869dup
NR_134950.2:n.3370+869dup
Search 100 bp 5'
Search 100 bp 3'