Canonical Allele Identifier: CA375262384

Gene: ABL1

Linked Data

• gnomAD v4: 9-130862794-C-A
• MyVariant Identifiers: chr9:g.133738181C>A (hg19) ; chr9:g.130862794C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862794C>A , CM000671.2:g.130862794C>A	GRCh38
NC_000009.11:g.133738181C>A , CM000671.1:g.133738181C>A	GRCh37
NC_000009.10:g.132728002C>A	NCBI36
NG_012034.1:g.153914C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000372348.9:c.638C>A	ENSP00000361423.2:p.Thr213Asn
ENST00000318560.6:c.581C>A MANE Select	ENSP00000323315.5:p.Thr194Asn
ENST00000372348.7:c.638C>A	ENSP00000361423.2:p.Thr213Asn
ENST00000318560.5:c.581C>A	ENSP00000323315.5:p.Thr194Asn
ENST00000372348.6:c.638C>A	ENSP00000361423.2:p.Thr213Asn
NM_005157.5:c.581C>A	NP_005148.2:p.Thr194Asn
NM_007313.2:c.638C>A	NP_009297.2:p.Thr213Asn
NM_005157.6:c.581C>A MANE Select	NP_005148.2:p.Thr194Asn
NM_007313.3:c.638C>A	NP_009297.2:p.Thr213Asn