Canonical Allele Identifier: CA1881474953
Gene: ABL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872465A= , CM000671.2:g.130872465A= GRCh38
NC_000009.11:g.133747852A= , CM000671.1:g.133747852A= GRCh37
NC_000009.10:g.132737673A= NCBI36
NG_012034.1:g.163585A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+252A= ENSP00000361423.2:n.964+252A=
ENST00000318560.6:c.907+252A= MANE Select ENSP00000323315.5:n.907+252A=
ENST00000372348.7:c.964+252A= ENSP00000361423.2:n.964+252A=
ENST00000318560.5:c.907+252A= ENSP00000323315.5:n.907+252A=
ENST00000372348.6:c.964+252A= ENSP00000361423.2:n.964+252A=
NM_005157.5:c.907+252A= NP_005148.2:n.907+252A=
NM_007313.2:c.964+252A= NP_009297.2:n.964+252A=
NM_005157.6:c.907+252A= MANE Select NP_005148.2:n.907+252A=
NM_007313.3:c.964+252A= NP_009297.2:n.964+252A=
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