Canonical Allele Identifier: CA1881476423
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873249_130873251delinsACT , CM000671.2:g.130873249_130873251delinsACT GRCh38
NC_000009.11:g.133748636_133748638delinsACT , CM000671.1:g.133748636_133748638delinsACT GRCh37
NC_000009.10:g.132738457_132738459delinsACT NCBI36
NG_012034.1:g.164369_164371delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.1142+212_1142+214delinsACT ENSP00000361423.2:n.1142+212_1142+214delinsACT
ENST00000318560.6:c.1085+212_1085+214delinsACT MANE Select ENSP00000323315.5:n.1085+212_1085+214delinsACT
ENST00000372348.7:c.1142+212_1142+214delinsACT ENSP00000361423.2:n.1142+212_1142+214delinsACT
ENST00000318560.5:c.1085+212_1085+214delinsACT ENSP00000323315.5:n.1085+212_1085+214delinsACT
ENST00000372348.6:c.1142+212_1142+214delinsACT ENSP00000361423.2:n.1142+212_1142+214delinsACT
NM_005157.5:c.1085+212_1085+214delinsACT NP_005148.2:n.1085+212_1085+214delinsACT
NM_007313.2:c.1142+212_1142+214delinsACT NP_009297.2:n.1142+212_1142+214delinsACT
NM_005157.6:c.1085+212_1085+214delinsACT MANE Select NP_005148.2:n.1085+212_1085+214delinsACT
NM_007313.3:c.1142+212_1142+214delinsACT NP_009297.2:n.1142+212_1142+214delinsACT