Canonical Allele Identifier: CA467395207
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133748410A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873023A>G , CM000671.2:g.130873023A>G GRCh38
NC_000009.11:g.133748410A>G , CM000671.1:g.133748410A>G GRCh37
NC_000009.10:g.132738231A>G NCBI36
NG_012034.1:g.164143A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1128A>G ENSP00000361423.2:p.Lys376=
ENST00000318560.6:c.1071A>G MANE Select ENSP00000323315.5:p.Lys357=
ENST00000372348.7:c.1128A>G ENSP00000361423.2:p.Lys376=
ENST00000318560.5:c.1071A>G ENSP00000323315.5:p.Lys357=
ENST00000372348.6:c.1128A>G ENSP00000361423.2:p.Lys376=
NM_005157.5:c.1071A>G NP_005148.2:p.Lys357=
NM_007313.2:c.1128A>G NP_009297.2:p.Lys376=
NM_005157.6:c.1071A>G MANE Select NP_005148.2:p.Lys357=
NM_007313.3:c.1128A>G NP_009297.2:p.Lys376=