Canonical Allele Identifier: CA2692152602

Gene: ABL1

Linked Data

• gnomAD v4: 9-130872340-GTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872341_130872342del , CM000671.2:g.130872341_130872342del	GRCh38
NC_000009.11:g.133747728_133747729del , CM000671.1:g.133747728_133747729del	GRCh37
NC_000009.10:g.132737549_132737550del	NCBI36
NG_012034.1:g.163461_163462del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.964+128_964+129del	ENSP00000361423.2:n.964+128_964+129del
ENST00000318560.6:c.907+128_907+129del MANE Select	ENSP00000323315.5:n.907+128_907+129del
ENST00000372348.7:c.964+128_964+129del	ENSP00000361423.2:n.964+128_964+129del
ENST00000318560.5:c.907+128_907+129del	ENSP00000323315.5:n.907+128_907+129del
ENST00000372348.6:c.964+128_964+129del	ENSP00000361423.2:n.964+128_964+129del
NM_005157.5:c.907+128_907+129del	NP_005148.2:n.907+128_907+129del
NM_007313.2:c.964+128_964+129del	NP_009297.2:n.964+128_964+129del
NM_005157.6:c.907+128_907+129del MANE Select	NP_005148.2:n.907+128_907+129del
NM_007313.3:c.964+128_964+129del	NP_009297.2:n.964+128_964+129del