Canonical Allele Identifier: CA5285316
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs768145590
ExAC: 9:133747612 CG / C
gnomAD v2: 9-133747612-CG-C
gnomAD v4: 9-130872225-CG-C
MyVariant Identifiers: chr9:g.133747613del (hg19) chr9:g.130872226del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872229del , CM000671.2:g.130872229del GRCh38
NC_000009.11:g.133747616del , CM000671.1:g.133747616del GRCh37
NC_000009.10:g.132737437del NCBI36
NG_012034.1:g.163349del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+16del ENSP00000361423.2:n.964+16del
ENST00000318560.6:c.907+16del MANE Select ENSP00000323315.5:n.907+16del
ENST00000372348.7:c.964+16del ENSP00000361423.2:n.964+16del
ENST00000318560.5:c.907+16del ENSP00000323315.5:n.907+16del
ENST00000372348.6:c.964+16del ENSP00000361423.2:n.964+16del
NM_005157.5:c.907+16del NP_005148.2:n.907+16del
NM_007313.2:c.964+16del NP_009297.2:n.964+16del
NM_005157.6:c.907+16del MANE Select NP_005148.2:n.907+16del
NM_007313.3:c.964+16del NP_009297.2:n.964+16del
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