Canonical Allele Identifier: CA1129551845
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1831266813
gnomAD v3: 9-130872378-T-TA
gnomAD v4: 9-130872378-T-TA
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872378_130872379insA , CM000671.2:g.130872378_130872379insA GRCh38
NC_000009.11:g.133747765_133747766insA , CM000671.1:g.133747765_133747766insA GRCh37
NC_000009.10:g.132737586_132737587insA NCBI36
NG_012034.1:g.163498_163499insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+165_964+166insA ENSP00000361423.2:n.964+165_964+166insA
ENST00000318560.6:c.907+165_907+166insA MANE Select ENSP00000323315.5:n.907+165_907+166insA
ENST00000372348.7:c.964+165_964+166insA ENSP00000361423.2:n.964+165_964+166insA
ENST00000318560.5:c.907+165_907+166insA ENSP00000323315.5:n.907+165_907+166insA
ENST00000372348.6:c.964+165_964+166insA ENSP00000361423.2:n.964+165_964+166insA
NM_005157.5:c.907+165_907+166insA NP_005148.2:n.907+165_907+166insA
NM_007313.2:c.964+165_964+166insA NP_009297.2:n.964+165_964+166insA
NM_005157.6:c.907+165_907+166insA MANE Select NP_005148.2:n.907+165_907+166insA
NM_007313.3:c.964+165_964+166insA NP_009297.2:n.964+165_964+166insA
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