Canonical Allele Identifier: CA1881476000
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872897T= , CM000671.2:g.130872897T= GRCh38
NC_000009.11:g.133748284T= , CM000671.1:g.133748284T= GRCh37
NC_000009.10:g.132738105T= NCBI36
NG_012034.1:g.164017T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.1002T= ENSP00000361423.2:p.Thr334=
ENST00000318560.6:c.945T= MANE Select ENSP00000323315.5:p.Thr315=
ENST00000372348.7:c.1002T= ENSP00000361423.2:p.Thr334=
ENST00000318560.5:c.945T= ENSP00000323315.5:p.Thr315=
ENST00000372348.6:c.1002T= ENSP00000361423.2:p.Thr334=
NM_005157.5:c.945T= NP_005148.2:p.Thr315=
NM_007313.2:c.1002T= NP_009297.2:p.Thr334=
NM_005157.6:c.945T= MANE Select NP_005148.2:p.Thr315=
NM_007313.3:c.1002T= NP_009297.2:p.Thr334=