Canonical Allele Identifier: CA5285303
Gene: ABL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2968850
ClinVar RCV Id: RCV003829496
dbSNP Id: rs761756351
ExAC: 9:133747498 G / GT
gnomAD v2: 9-133747498-G-GT
gnomAD v3: 9-130872111-G-GT
gnomAD v4: 9-130872111-G-GT
MyVariant Identifiers: chr9:g.133747499_133747500insT (hg19) chr9:g.133747498_133747499insT (hg19) chr9:g.130872112_130872113insT (hg38) chr9:g.130872111_130872112insT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872118dup , CM000671.2:g.130872118dup GRCh38
NC_000009.11:g.133747505dup , CM000671.1:g.133747505dup GRCh37
NC_000009.10:g.132737326dup NCBI36
NG_012034.1:g.163238dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.880-11dup ENSP00000361423.2:n.880-11dup
ENST00000318560.6:c.823-11dup MANE Select ENSP00000323315.5:n.823-11dup
ENST00000372348.7:c.880-11dup ENSP00000361423.2:n.880-11dup
ENST00000318560.5:c.823-11dup ENSP00000323315.5:n.823-11dup
ENST00000372348.6:c.880-11dup ENSP00000361423.2:n.880-11dup
NM_005157.5:c.823-11dup NP_005148.2:n.823-11dup
NM_007313.2:c.880-11dup NP_009297.2:n.880-11dup
NM_005157.6:c.823-11dup MANE Select NP_005148.2:n.823-11dup
NM_007313.3:c.880-11dup NP_009297.2:n.880-11dup
Search 100 bp 5'
Search 100 bp 3'