Canonical Allele Identifier: CA200644958
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs950994343
MyVariant Identifiers: chr9:g.133747370del (hg19) chr9:g.130871983del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130871984del , CM000671.2:g.130871984del GRCh38
NC_000009.11:g.133747371del , CM000671.1:g.133747371del GRCh37
NC_000009.10:g.132737192del NCBI36
NG_012034.1:g.163104del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.880-145del ENSP00000361423.2:n.880-145del
ENST00000318560.6:c.823-145del MANE Select ENSP00000323315.5:n.823-145del
ENST00000372348.7:c.880-145del ENSP00000361423.2:n.880-145del
ENST00000318560.5:c.823-145del ENSP00000323315.5:n.823-145del
ENST00000372348.6:c.880-145del ENSP00000361423.2:n.880-145del
NM_005157.5:c.823-145del NP_005148.2:n.823-145del
NM_007313.2:c.880-145del NP_009297.2:n.880-145del
NM_005157.6:c.823-145del MANE Select NP_005148.2:n.823-145del
NM_007313.3:c.880-145del NP_009297.2:n.880-145del
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