Canonical Allele Identifier: CA122590
Gene: ABL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12629
ClinVar RCV Id: RCV000420800
dbSNP Id: rs121913457
COSMIC: COSM12578
CIViC: CA122590

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873004T>C , CM000671.2:g.130873004T>C GRCh38
NC_000009.11:g.133748391T>C , CM000671.1:g.133748391T>C GRCh37
NC_000009.10:g.132738212T>C NCBI36
NG_012034.1:g.164124T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000318560.6:c.1052T>C MANE Select ENSP00000323315.5:p.Met351Thr
ENST00000372348.7:c.1109T>C ENSP00000361423.2:p.Met370Thr
ENST00000318560.5:c.1052T>C ENSP00000323315.5:p.Met351Thr
ENST00000372348.6:c.1109T>C ENSP00000361423.2:p.Met370Thr
NM_005157.5:c.1052T>C NP_005148.2:p.Met351Thr
NM_007313.2:c.1109T>C NP_009297.2:p.Met370Thr
NM_005157.6:c.1052T>C MANE Select NP_005148.2:p.Met351Thr
NM_007313.3:c.1109T>C NP_009297.2:p.Met370Thr