Canonical Allele Identifier: CA1129551878
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1831268701
gnomAD v3: 9-130872487-CTT-C
gnomAD v4: 9-130872487-CTT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872488_130872489del , CM000671.2:g.130872488_130872489del GRCh38
NC_000009.11:g.133747875_133747876del , CM000671.1:g.133747875_133747876del GRCh37
NC_000009.10:g.132737696_132737697del NCBI36
NG_012034.1:g.163608_163609del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+275_964+276del ENSP00000361423.2:n.964+275_964+276del
ENST00000318560.6:c.907+275_907+276del MANE Select ENSP00000323315.5:n.907+275_907+276del
ENST00000372348.7:c.964+275_964+276del ENSP00000361423.2:n.964+275_964+276del
ENST00000318560.5:c.907+275_907+276del ENSP00000323315.5:n.907+275_907+276del
ENST00000372348.6:c.964+275_964+276del ENSP00000361423.2:n.964+275_964+276del
NM_005157.5:c.907+275_907+276del NP_005148.2:n.907+275_907+276del
NM_007313.2:c.964+275_964+276del NP_009297.2:n.964+275_964+276del
NM_005157.6:c.907+275_907+276del MANE Select NP_005148.2:n.907+275_907+276del
NM_007313.3:c.964+275_964+276del NP_009297.2:n.964+275_964+276del
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