Canonical Allele Identifier: CA1881476402
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873209C= , CM000671.2:g.130873209C= GRCh38
NC_000009.11:g.133748596C= , CM000671.1:g.133748596C= GRCh37
NC_000009.10:g.132738417C= NCBI36
NG_012034.1:g.164329C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.1142+172C= ENSP00000361423.2:n.1142+172C=
ENST00000318560.6:c.1085+172C= MANE Select ENSP00000323315.5:n.1085+172C=
ENST00000372348.7:c.1142+172C= ENSP00000361423.2:n.1142+172C=
ENST00000318560.5:c.1085+172C= ENSP00000323315.5:n.1085+172C=
ENST00000372348.6:c.1142+172C= ENSP00000361423.2:n.1142+172C=
NM_005157.5:c.1085+172C= NP_005148.2:n.1085+172C=
NM_007313.2:c.1142+172C= NP_009297.2:n.1142+172C=
NM_005157.6:c.1085+172C= MANE Select NP_005148.2:n.1085+172C=
NM_007313.3:c.1142+172C= NP_009297.2:n.1142+172C=