Canonical Allele Identifier: CA3169188287
Community Standard Title: NM_005157.6(ABL1):c.1015G= (p.Val339=)
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872967G= , CM000671.2:g.130872967G= GRCh38
NC_000009.11:g.133748354G= , CM000671.1:g.133748354G= GRCh37
NC_000009.10:g.132738175G= NCBI36
NG_012034.1:g.164087G=

Transcript Alleles

HGVS Amino-acid Change
NM_005157.6:c.1015G= MANE Select NP_005148.2:p.Val339=
ENST00000318560.6:c.1015G= MANE Select ENSP00000323315.5:p.Val339=
NM_005157.5:c.1015G= NP_005148.2:p.Val339=
NM_007313.2:c.1072G= NP_009297.2:p.Val358=
NM_007313.3:c.1072G= NP_009297.2:p.Val358=
ENST00000318560.5:c.1015G= ENSP00000323315.5:p.Val339=
ENST00000372348.6:c.1072G= ENSP00000361423.2:p.Val358=
ENST00000372348.7:c.1072G= ENSP00000361423.2:p.Val358=
ENST00000372348.9:c.1072G= ENSP00000361423.2:p.Val358=