Canonical Allele Identifier: CA5285371

Gene: ABL1

Linked Data

• dbSNP Id: rs548954575
• ExAC: 9:133748435 G / A
• gnomAD v2: 9-133748435-G-A
• gnomAD v3: 9-130873048-G-A
• gnomAD v4: 9-130873048-G-A
• MyVariant Identifiers: chr9:g.133748435G>A (hg19) ; chr9:g.130873048G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130873048G>A , CM000671.2:g.130873048G>A	GRCh38
NC_000009.11:g.133748435G>A , CM000671.1:g.133748435G>A	GRCh37
NC_000009.10:g.132738256G>A	NCBI36
NG_012034.1:g.164168G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.1142+11G>A	ENSP00000361423.2:n.1142+11G>A
ENST00000318560.6:c.1085+11G>A MANE Select	ENSP00000323315.5:n.1085+11G>A
ENST00000372348.7:c.1142+11G>A	ENSP00000361423.2:n.1142+11G>A
ENST00000318560.5:c.1085+11G>A	ENSP00000323315.5:n.1085+11G>A
ENST00000372348.6:c.1142+11G>A	ENSP00000361423.2:n.1142+11G>A
NM_005157.5:c.1085+11G>A	NP_005148.2:n.1085+11G>A
NM_007313.2:c.1142+11G>A	NP_009297.2:n.1142+11G>A
NM_005157.6:c.1085+11G>A MANE Select	NP_005148.2:n.1085+11G>A
NM_007313.3:c.1142+11G>A	NP_009297.2:n.1142+11G>A