Canonical Allele Identifier: CA2720749387
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs2132997875

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873075del , CM000671.2:g.130873075del GRCh38
NC_000009.11:g.133748462del , CM000671.1:g.133748462del GRCh37
NC_000009.10:g.132738283del NCBI36
NG_012034.1:g.164195del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.1142+38del ENSP00000361423.2:n.1142+38del
ENST00000318560.6:c.1085+38del MANE Select ENSP00000323315.5:n.1085+38del
ENST00000372348.7:c.1142+38del ENSP00000361423.2:n.1142+38del
ENST00000318560.5:c.1085+38del ENSP00000323315.5:n.1085+38del
ENST00000372348.6:c.1142+38del ENSP00000361423.2:n.1142+38del
NM_005157.5:c.1085+38del NP_005148.2:n.1085+38del
NM_007313.2:c.1142+38del NP_009297.2:n.1142+38del
NM_005157.6:c.1085+38del MANE Select NP_005148.2:n.1085+38del
NM_007313.3:c.1142+38del NP_009297.2:n.1142+38del