Canonical Allele Identifier: CA1129551869
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1831267558

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872411_130872414del , CM000671.2:g.130872411_130872414del GRCh38
NC_000009.11:g.133747798_133747801del , CM000671.1:g.133747798_133747801del GRCh37
NC_000009.10:g.132737619_132737622del NCBI36
NG_012034.1:g.163531_163534del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+198_964+201del ENSP00000361423.2:n.964+198_964+201del
ENST00000318560.6:c.907+198_907+201del MANE Select ENSP00000323315.5:n.907+198_907+201del
ENST00000372348.7:c.964+198_964+201del ENSP00000361423.2:n.964+198_964+201del
ENST00000318560.5:c.907+198_907+201del ENSP00000323315.5:n.907+198_907+201del
ENST00000372348.6:c.964+198_964+201del ENSP00000361423.2:n.964+198_964+201del
NM_005157.5:c.907+198_907+201del NP_005148.2:n.907+198_907+201del
NM_007313.2:c.964+198_964+201del NP_009297.2:n.964+198_964+201del
NM_005157.6:c.907+198_907+201del MANE Select NP_005148.2:n.907+198_907+201del
NM_007313.3:c.964+198_964+201del NP_009297.2:n.964+198_964+201del