Canonical Allele Identifier: CA375251154
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133753880A>C (hg19) chr9:g.130878493A>C (hg38)
CIViC: CA375251154
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130878493A>C , CM000671.2:g.130878493A>C GRCh38
NC_000009.11:g.133753880A>C , CM000671.1:g.133753880A>C GRCh37
NC_000009.10:g.132743701A>C NCBI36
NG_012034.1:g.169613A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1406A>C ENSP00000361423.2:p.Glu469Ala
ENST00000318560.6:c.1349A>C MANE Select ENSP00000323315.5:p.Glu450Ala
ENST00000372348.7:c.1406A>C ENSP00000361423.2:p.Glu469Ala
ENST00000318560.5:c.1349A>C ENSP00000323315.5:p.Glu450Ala
ENST00000372348.6:c.1406A>C ENSP00000361423.2:p.Glu469Ala
NM_005157.5:c.1349A>C NP_005148.2:p.Glu450Ala
NM_007313.2:c.1406A>C NP_009297.2:p.Glu469Ala
NM_005157.6:c.1349A>C MANE Select NP_005148.2:p.Glu450Ala
NM_007313.3:c.1406A>C NP_009297.2:p.Glu469Ala
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