Canonical Allele Identifier: CA5285419
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs764105054
ExAC: 9:133753853 C / T
gnomAD v2: 9-133753853-C-T
gnomAD v4: 9-130878466-C-T
COSMIC: COSM308520 COSM3329171 COSM3329172
MyVariant Identifiers: chr9:g.133753853C>T (hg19) chr9:g.130878466C>T (hg38)
CIViC: CA5285419
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130878466C>T , CM000671.2:g.130878466C>T GRCh38
NC_000009.11:g.133753853C>T , CM000671.1:g.133753853C>T GRCh37
NC_000009.10:g.132743674C>T NCBI36
NG_012034.1:g.169586C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1379C>T ENSP00000361423.2:p.Pro460Leu
ENST00000318560.6:c.1322C>T MANE Select ENSP00000323315.5:p.Pro441Leu
ENST00000372348.7:c.1379C>T ENSP00000361423.2:p.Pro460Leu
ENST00000318560.5:c.1322C>T ENSP00000323315.5:p.Pro441Leu
ENST00000372348.6:c.1379C>T ENSP00000361423.2:p.Pro460Leu
NM_005157.5:c.1322C>T NP_005148.2:p.Pro441Leu
NM_007313.2:c.1379C>T NP_009297.2:p.Pro460Leu
NM_005157.6:c.1322C>T MANE Select NP_005148.2:p.Pro441Leu
NM_007313.3:c.1379C>T NP_009297.2:p.Pro460Leu
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