Canonical Allele Identifier: CA860511638

Gene: ABL1

Linked Data

• dbSNP Id: rs1479715064
• gnomAD v3: 9-130872423-ATG-A
• gnomAD v4: 9-130872423-ATG-A
• MyVariant Identifiers: chr9:g.133747811_133747812del (hg19) ; chr9:g.130872424_130872425del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872426_130872427del , CM000671.2:g.130872426_130872427del	GRCh38
NC_000009.11:g.133747813_133747814del , CM000671.1:g.133747813_133747814del	GRCh37
NC_000009.10:g.132737634_132737635del	NCBI36
NG_012034.1:g.163546_163547del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.964+213_964+214del	ENSP00000361423.2:n.964+213_964+214del
ENST00000318560.6:c.907+213_907+214del MANE Select	ENSP00000323315.5:n.907+213_907+214del
ENST00000372348.7:c.964+213_964+214del	ENSP00000361423.2:n.964+213_964+214del
ENST00000318560.5:c.907+213_907+214del	ENSP00000323315.5:n.907+213_907+214del
ENST00000372348.6:c.964+213_964+214del	ENSP00000361423.2:n.964+213_964+214del
NM_005157.5:c.907+213_907+214del	NP_005148.2:n.907+213_907+214del
NM_007313.2:c.964+213_964+214del	NP_009297.2:n.964+213_964+214del
NM_005157.6:c.907+213_907+214del MANE Select	NP_005148.2:n.907+213_907+214del
NM_007313.3:c.964+213_964+214del	NP_009297.2:n.964+213_964+214del