Canonical Allele Identifier: CA467395158
Community Standard Title: NM_005157.6(ABL1):c.1020G>C (p.Leu340=)
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872972G>C , CM000671.2:g.130872972G>C GRCh38
NC_000009.11:g.133748359G>C , CM000671.1:g.133748359G>C GRCh37
NC_000009.10:g.132738180G>C NCBI36
NG_012034.1:g.164092G>C

Transcript Alleles

HGVS Amino-acid Change
NM_005157.6:c.1020G>C MANE Select NP_005148.2:p.Leu340=
ENST00000318560.6:c.1020G>C MANE Select ENSP00000323315.5:p.Leu340=
NM_005157.5:c.1020G>C NP_005148.2:p.Leu340=
NM_007313.2:c.1077G>C NP_009297.2:p.Leu359=
NM_007313.3:c.1077G>C NP_009297.2:p.Leu359=
ENST00000318560.5:c.1020G>C ENSP00000323315.5:p.Leu340=
ENST00000372348.6:c.1077G>C ENSP00000361423.2:p.Leu359=
ENST00000372348.7:c.1077G>C ENSP00000361423.2:p.Leu359=
ENST00000372348.9:c.1077G>C ENSP00000361423.2:p.Leu359=