Canonical Allele Identifier: CA16602557
Gene: ABL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 376096
ClinVar RCV Id: RCV000437822
dbSNP Id: rs121913452
COSMIC: COSM12605

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873027T>G , CM000671.2:g.130873027T>G GRCh38
NC_000009.11:g.133748414T>G , CM000671.1:g.133748414T>G GRCh37
NC_000009.10:g.132738235T>G NCBI36
NG_012034.1:g.164147T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1132T>G ENSP00000361423.2:p.Phe378Val
ENST00000318560.6:c.1075T>G MANE Select ENSP00000323315.5:p.Phe359Val
ENST00000372348.7:c.1132T>G ENSP00000361423.2:p.Phe378Val
ENST00000318560.5:c.1075T>G ENSP00000323315.5:p.Phe359Val
ENST00000372348.6:c.1132T>G ENSP00000361423.2:p.Phe378Val
NM_005157.5:c.1075T>G NP_005148.2:p.Phe359Val
NM_007313.2:c.1132T>G NP_009297.2:p.Phe378Val
NM_005157.6:c.1075T>G MANE Select NP_005148.2:p.Phe359Val
NM_007313.3:c.1132T>G NP_009297.2:p.Phe378Val