Canonical Allele Identifier: CA375251559
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133755469C>G (hg19) chr9:g.130880082C>G (hg38)
CIViC: CA375251559
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130880082C>G , CM000671.2:g.130880082C>G GRCh38
NC_000009.11:g.133755469C>G , CM000671.1:g.133755469C>G GRCh37
NC_000009.10:g.132745290C>G NCBI36
NG_012034.1:g.171202C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1495C>G ENSP00000361423.2:p.Pro499Ala
ENST00000318560.6:c.1438C>G MANE Select ENSP00000323315.5:p.Pro480Ala
ENST00000372348.7:c.1495C>G ENSP00000361423.2:p.Pro499Ala
ENST00000318560.5:c.1438C>G ENSP00000323315.5:p.Pro480Ala
ENST00000372348.6:c.1495C>G ENSP00000361423.2:p.Pro499Ala
NM_005157.5:c.1438C>G NP_005148.2:p.Pro480Ala
NM_007313.2:c.1495C>G NP_009297.2:p.Pro499Ala
NM_005157.6:c.1438C>G MANE Select NP_005148.2:p.Pro480Ala
NM_007313.3:c.1495C>G NP_009297.2:p.Pro499Ala
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