Canonical Allele Identifier: CA5285372

Gene: ABL1

Linked Data

• dbSNP Id: rs763402515
• ExAC: 9:133748437 C / T
• gnomAD v2: 9-133748437-C-T
• gnomAD v4: 9-130873050-C-T
• MyVariant Identifiers: chr9:g.133748437C>T (hg19) ; chr9:g.130873050C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130873050C>T , CM000671.2:g.130873050C>T	GRCh38
NC_000009.11:g.133748437C>T , CM000671.1:g.133748437C>T	GRCh37
NC_000009.10:g.132738258C>T	NCBI36
NG_012034.1:g.164170C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.1142+13C>T	ENSP00000361423.2:n.1142+13C>T
ENST00000318560.6:c.1085+13C>T MANE Select	ENSP00000323315.5:n.1085+13C>T
ENST00000372348.7:c.1142+13C>T	ENSP00000361423.2:n.1142+13C>T
ENST00000318560.5:c.1085+13C>T	ENSP00000323315.5:n.1085+13C>T
ENST00000372348.6:c.1142+13C>T	ENSP00000361423.2:n.1142+13C>T
NM_005157.5:c.1085+13C>T	NP_005148.2:n.1085+13C>T
NM_007313.2:c.1142+13C>T	NP_009297.2:n.1142+13C>T
NM_005157.6:c.1085+13C>T MANE Select	NP_005148.2:n.1085+13C>T
NM_007313.3:c.1142+13C>T	NP_009297.2:n.1142+13C>T