Canonical Allele Identifier: CA1881476292
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1831281054

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873099_130873100dup , CM000671.2:g.130873099_130873100dup GRCh38
NC_000009.11:g.133748486_133748487dup , CM000671.1:g.133748486_133748487dup GRCh37
NC_000009.10:g.132738307_132738308dup NCBI36
NG_012034.1:g.164219_164220dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.1142+62_1142+63dup ENSP00000361423.2:n.1142+62_1142+63dup
ENST00000318560.6:c.1085+62_1085+63dup MANE Select ENSP00000323315.5:n.1085+62_1085+63dup
ENST00000372348.7:c.1142+62_1142+63dup ENSP00000361423.2:n.1142+62_1142+63dup
ENST00000318560.5:c.1085+62_1085+63dup ENSP00000323315.5:n.1085+62_1085+63dup
ENST00000372348.6:c.1142+62_1142+63dup ENSP00000361423.2:n.1142+62_1142+63dup
NM_005157.5:c.1085+62_1085+63dup NP_005148.2:n.1085+62_1085+63dup
NM_007313.2:c.1142+62_1142+63dup NP_009297.2:n.1142+62_1142+63dup
NM_005157.6:c.1085+62_1085+63dup MANE Select NP_005148.2:n.1085+62_1085+63dup
NM_007313.3:c.1142+62_1142+63dup NP_009297.2:n.1142+62_1142+63dup