Canonical Allele Identifier: CA1881476162
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873010A= , CM000671.2:g.130873010A= GRCh38
NC_000009.11:g.133748397A= , CM000671.1:g.133748397A= GRCh37
NC_000009.10:g.132738218A= NCBI36
NG_012034.1:g.164130A=

Transcript Alleles

HGVS Amino-acid change
ENST00000318560.6:c.1058A= MANE Select ENSP00000323315.5:p.Tyr353=
ENST00000372348.7:c.1115A= ENSP00000361423.2:p.Tyr372=
ENST00000318560.5:c.1058A= ENSP00000323315.5:p.Tyr353=
ENST00000372348.6:c.1115A= ENSP00000361423.2:p.Tyr372=
NM_005157.5:c.1058A= NP_005148.2:p.Tyr353=
NM_007313.2:c.1115A= NP_009297.2:p.Tyr372=
NM_005157.6:c.1058A= MANE Select NP_005148.2:p.Tyr353=
NM_007313.3:c.1115A= NP_009297.2:p.Tyr372=