Canonical Allele Identifier: CA1881443123
Gene: ABL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130852664G>C , CM000671.2:g.130852664G>C GRCh38
NC_000009.11:g.133728051G>C , CM000671.1:g.133728051G>C GRCh37
NC_000009.10:g.132717872G>C NCBI36
NG_012034.1:g.143784G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.137-1400G>C ENSP00000361423.2:n.137-1400G>C
ENST00000318560.6:c.80-1400G>C MANE Select ENSP00000323315.5:n.80-1400G>C
ENST00000372348.7:c.137-1400G>C ENSP00000361423.2:n.137-1400G>C
ENST00000318560.5:c.80-1400G>C ENSP00000323315.5:n.80-1400G>C
ENST00000372348.6:c.137-1400G>C ENSP00000361423.2:n.137-1400G>C
ENST00000393293.4:c.137-1403G>C ENSP00000376971.4:n.137-1403G>C
NM_005157.5:c.80-1400G>C NP_005148.2:n.80-1400G>C
NM_007313.2:c.137-1400G>C NP_009297.2:n.137-1400G>C
NM_005157.6:c.80-1400G>C MANE Select NP_005148.2:n.80-1400G>C
NM_007313.3:c.137-1400G>C NP_009297.2:n.137-1400G>C