Canonical Allele Identifier: CA1881476217
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873048G= , CM000671.2:g.130873048G= GRCh38
NC_000009.11:g.133748435G= , CM000671.1:g.133748435G= GRCh37
NC_000009.10:g.132738256G= NCBI36
NG_012034.1:g.164168G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1142+11G= ENSP00000361423.2:n.1142+11G=
ENST00000318560.6:c.1085+11G= MANE Select ENSP00000323315.5:n.1085+11G=
ENST00000372348.7:c.1142+11G= ENSP00000361423.2:n.1142+11G=
ENST00000318560.5:c.1085+11G= ENSP00000323315.5:n.1085+11G=
ENST00000372348.6:c.1142+11G= ENSP00000361423.2:n.1142+11G=
NM_005157.5:c.1085+11G= NP_005148.2:n.1085+11G=
NM_007313.2:c.1142+11G= NP_009297.2:n.1142+11G=
NM_005157.6:c.1085+11G= MANE Select NP_005148.2:n.1085+11G=
NM_007313.3:c.1142+11G= NP_009297.2:n.1142+11G=