Canonical Allele Identifier: CA375249885
Gene: ABL1 HGNC NCBI

Linked Data

COSMIC: COSM49071
MyVariant Identifiers: chr9:g.133750319C>A (hg19) chr9:g.130874932C>A (hg38)
CIViC: CA375249885
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130874932C>A , CM000671.2:g.130874932C>A GRCh38
NC_000009.11:g.133750319C>A , CM000671.1:g.133750319C>A GRCh37
NC_000009.10:g.132740140C>A NCBI36
NG_012034.1:g.166052C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1207C>A ENSP00000361423.2:p.Leu403Met
ENST00000318560.6:c.1150C>A MANE Select ENSP00000323315.5:p.Leu384Met
ENST00000372348.7:c.1207C>A ENSP00000361423.2:p.Leu403Met
ENST00000318560.5:c.1150C>A ENSP00000323315.5:p.Leu384Met
ENST00000372348.6:c.1207C>A ENSP00000361423.2:p.Leu403Met
NM_005157.5:c.1150C>A NP_005148.2:p.Leu384Met
NM_007313.2:c.1207C>A NP_009297.2:p.Leu403Met
NM_005157.6:c.1150C>A MANE Select NP_005148.2:p.Leu384Met
NM_007313.3:c.1207C>A NP_009297.2:p.Leu403Met
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