Canonical Allele Identifier: CA2692152644

Gene: ABL1

Linked Data

• gnomAD v4: 9-130872363-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872363_130872364insA , CM000671.2:g.130872363_130872364insA	GRCh38
NC_000009.11:g.133747750_133747751insA , CM000671.1:g.133747750_133747751insA	GRCh37
NC_000009.10:g.132737571_132737572insA	NCBI36
NG_012034.1:g.163483_163484insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.964+150_964+151insA	ENSP00000361423.2:n.964+150_964+151insA
ENST00000318560.6:c.907+150_907+151insA MANE Select	ENSP00000323315.5:n.907+150_907+151insA
ENST00000372348.7:c.964+150_964+151insA	ENSP00000361423.2:n.964+150_964+151insA
ENST00000318560.5:c.907+150_907+151insA	ENSP00000323315.5:n.907+150_907+151insA
ENST00000372348.6:c.964+150_964+151insA	ENSP00000361423.2:n.964+150_964+151insA
NM_005157.5:c.907+150_907+151insA	NP_005148.2:n.907+150_907+151insA
NM_007313.2:c.964+150_964+151insA	NP_009297.2:n.964+150_964+151insA
NM_005157.6:c.907+150_907+151insA MANE Select	NP_005148.2:n.907+150_907+151insA
NM_007313.3:c.964+150_964+151insA	NP_009297.2:n.964+150_964+151insA