Canonical Allele Identifier: CA2720747412
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs2132994999

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872252_130872262del , CM000671.2:g.130872252_130872262del GRCh38
NC_000009.11:g.133747639_133747649del , CM000671.1:g.133747639_133747649del GRCh37
NC_000009.10:g.132737460_132737470del NCBI36
NG_012034.1:g.163372_163382del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+39_964+49del ENSP00000361423.2:n.964+39_964+49del
ENST00000318560.6:c.907+39_907+49del MANE Select ENSP00000323315.5:n.907+39_907+49del
ENST00000372348.7:c.964+39_964+49del ENSP00000361423.2:n.964+39_964+49del
ENST00000318560.5:c.907+39_907+49del ENSP00000323315.5:n.907+39_907+49del
ENST00000372348.6:c.964+39_964+49del ENSP00000361423.2:n.964+39_964+49del
NM_005157.5:c.907+39_907+49del NP_005148.2:n.907+39_907+49del
NM_007313.2:c.964+39_964+49del NP_009297.2:n.964+39_964+49del
NM_005157.6:c.907+39_907+49del MANE Select NP_005148.2:n.907+39_907+49del
NM_007313.3:c.964+39_964+49del NP_009297.2:n.964+39_964+49del