Canonical Allele Identifier: CA3171396461
Community Standard Title: NM_005157.6(ABL1):c.1013T= (p.Val338=)
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872965T= , CM000671.2:g.130872965T= GRCh38
NC_000009.11:g.133748352T= , CM000671.1:g.133748352T= GRCh37
NC_000009.10:g.132738173T= NCBI36
NG_012034.1:g.164085T=

Transcript Alleles

HGVS Amino-acid Change
NM_005157.6:c.1013T= MANE Select NP_005148.2:p.Val338=
ENST00000318560.6:c.1013T= MANE Select ENSP00000323315.5:p.Val338=
NM_005157.5:c.1013T= NP_005148.2:p.Val338=
NM_007313.2:c.1070T= NP_009297.2:p.Val357=
NM_007313.3:c.1070T= NP_009297.2:p.Val357=
ENST00000318560.5:c.1013T= ENSP00000323315.5:p.Val338=
ENST00000372348.6:c.1070T= ENSP00000361423.2:p.Val357=
ENST00000372348.7:c.1070T= ENSP00000361423.2:p.Val357=
ENST00000372348.9:c.1070T= ENSP00000361423.2:p.Val357=