Canonical Allele Identifier: CA1881463460
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862970T= , CM000671.2:g.130862970T= GRCh38
NC_000009.11:g.133738357T= , CM000671.1:g.133738357T= GRCh37
NC_000009.10:g.132728178T= NCBI36
NG_012034.1:g.154090T=

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.814T= ENSP00000361423.2:p.Tyr272=
ENST00000318560.6:c.757T= MANE Select ENSP00000323315.5:p.Tyr253=
ENST00000372348.7:c.814T= ENSP00000361423.2:p.Tyr272=
ENST00000318560.5:c.757T= ENSP00000323315.5:p.Tyr253=
ENST00000372348.6:c.814T= ENSP00000361423.2:p.Tyr272=
NM_005157.5:c.757T= NP_005148.2:p.Tyr253=
NM_007313.2:c.814T= NP_009297.2:p.Tyr272=
NM_005157.6:c.757T= MANE Select NP_005148.2:p.Tyr253=
NM_007313.3:c.814T= NP_009297.2:p.Tyr272=