Canonical Allele Identifier: CA1881476347
Gene: ABL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873150T= , CM000671.2:g.130873150T= GRCh38
NC_000009.11:g.133748537T= , CM000671.1:g.133748537T= GRCh37
NC_000009.10:g.132738358T= NCBI36
NG_012034.1:g.164270T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.1142+113T= ENSP00000361423.2:n.1142+113T=
ENST00000318560.6:c.1085+113T= MANE Select ENSP00000323315.5:n.1085+113T=
ENST00000372348.7:c.1142+113T= ENSP00000361423.2:n.1142+113T=
ENST00000318560.5:c.1085+113T= ENSP00000323315.5:n.1085+113T=
ENST00000372348.6:c.1142+113T= ENSP00000361423.2:n.1142+113T=
NM_005157.5:c.1085+113T= NP_005148.2:n.1085+113T=
NM_007313.2:c.1142+113T= NP_009297.2:n.1142+113T=
NM_005157.6:c.1085+113T= MANE Select NP_005148.2:n.1085+113T=
NM_007313.3:c.1142+113T= NP_009297.2:n.1142+113T=
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