Canonical Allele Identifier: CA1881474755
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872200G= , CM000671.2:g.130872200G= GRCh38
NC_000009.11:g.133747587G= , CM000671.1:g.133747587G= GRCh37
NC_000009.10:g.132737408G= NCBI36
NG_012034.1:g.163320G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.951G= ENSP00000361423.2:p.Leu317=
ENST00000318560.6:c.894G= MANE Select ENSP00000323315.5:p.Leu298=
ENST00000372348.7:c.951G= ENSP00000361423.2:p.Leu317=
ENST00000318560.5:c.894G= ENSP00000323315.5:p.Leu298=
ENST00000372348.6:c.951G= ENSP00000361423.2:p.Leu317=
NM_005157.5:c.894G= NP_005148.2:p.Leu298=
NM_007313.2:c.951G= NP_009297.2:p.Leu317=
NM_005157.6:c.894G= MANE Select NP_005148.2:p.Leu298=
NM_007313.3:c.951G= NP_009297.2:p.Leu317=