Canonical Allele Identifier: CA375263246

Gene: ABL1

Linked Data

• gnomAD v4: 9-130862961-G-T
• MyVariant Identifiers: chr9:g.133738348G>T (hg19) ; chr9:g.130862961G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862961G>T , CM000671.2:g.130862961G>T	GRCh38
NC_000009.11:g.133738348G>T , CM000671.1:g.133738348G>T	GRCh37
NC_000009.10:g.132728169G>T	NCBI36
NG_012034.1:g.154081G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000372348.9:c.805G>T	ENSP00000361423.2:p.Gly269Trp
ENST00000318560.6:c.748G>T MANE Select	ENSP00000323315.5:p.Gly250Trp
ENST00000372348.7:c.805G>T	ENSP00000361423.2:p.Gly269Trp
ENST00000318560.5:c.748G>T	ENSP00000323315.5:p.Gly250Trp
ENST00000372348.6:c.805G>T	ENSP00000361423.2:p.Gly269Trp
NM_005157.5:c.748G>T	NP_005148.2:p.Gly250Trp
NM_007313.2:c.805G>T	NP_009297.2:p.Gly269Trp
NM_005157.6:c.748G>T MANE Select	NP_005148.2:p.Gly250Trp
NM_007313.3:c.805G>T	NP_009297.2:p.Gly269Trp