Canonical Allele Identifier: CA375263518

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133738415C>T (hg19) ; chr9:g.130863028C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130863028C>T , CM000671.2:g.130863028C>T	GRCh38
NC_000009.11:g.133738415C>T , CM000671.1:g.133738415C>T	GRCh37
NC_000009.10:g.132728236C>T	NCBI36
NG_012034.1:g.154148C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.872C>T	ENSP00000361423.2:p.Thr291Ile
ENST00000318560.6:c.815C>T MANE Select	ENSP00000323315.5:p.Thr272Ile
ENST00000372348.7:c.872C>T	ENSP00000361423.2:p.Thr291Ile
ENST00000318560.5:c.815C>T	ENSP00000323315.5:p.Thr272Ile
ENST00000372348.6:c.872C>T	ENSP00000361423.2:p.Thr291Ile
NM_005157.5:c.815C>T	NP_005148.2:p.Thr272Ile
NM_007313.2:c.872C>T	NP_009297.2:p.Thr291Ile
NM_005157.6:c.815C>T MANE Select	NP_005148.2:p.Thr272Ile
NM_007313.3:c.872C>T	NP_009297.2:p.Thr291Ile