Canonical Allele Identifier: CA16602551
Gene: ABL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 376090
ClinVar RCV Id: RCV000432426
dbSNP Id: rs121913448
gnomAD v4: 9-130862976-G-A
COSMIC: COSM12573
MyVariant Identifiers: chr9:g.133738363G>A (hg19) chr9:g.130862976G>A (hg38)
CIViC: CA16602551
PubMed: PMID:11423618 PMID:11567109 PMID:11853795 PMID:11861307 PMID:11964322 PMID:12399961 PMID:12623848 PMID:14745431 PMID:15194504 PMID:18757400 PMID:21509757 PMID:22210874 PMID:22912393 PMID:23676790 PMID:24236021 PMID:25157968
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862976G>A , CM000671.2:g.130862976G>A GRCh38
NC_000009.11:g.133738363G>A , CM000671.1:g.133738363G>A GRCh37
NC_000009.10:g.132728184G>A NCBI36
NG_012034.1:g.154096G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.820G>A ENSP00000361423.2:p.Glu274Lys
ENST00000318560.6:c.763G>A MANE Select ENSP00000323315.5:p.Glu255Lys
ENST00000372348.7:c.820G>A ENSP00000361423.2:p.Glu274Lys
ENST00000318560.5:c.763G>A ENSP00000323315.5:p.Glu255Lys
ENST00000372348.6:c.820G>A ENSP00000361423.2:p.Glu274Lys
NM_005157.5:c.763G>A NP_005148.2:p.Glu255Lys
NM_007313.2:c.820G>A NP_009297.2:p.Glu274Lys
NM_005157.6:c.763G>A MANE Select NP_005148.2:p.Glu255Lys
NM_007313.3:c.820G>A NP_009297.2:p.Glu274Lys
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