Canonical Allele Identifier: CA2692152844

Gene: ABL1

Linked Data

• gnomAD v4: 9-130873189-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130873189T>C , CM000671.2:g.130873189T>C	GRCh38
NC_000009.11:g.133748576T>C , CM000671.1:g.133748576T>C	GRCh37
NC_000009.10:g.132738397T>C	NCBI36
NG_012034.1:g.164309T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.1142+152T>C	ENSP00000361423.2:n.1142+152T>C
ENST00000318560.6:c.1085+152T>C MANE Select	ENSP00000323315.5:n.1085+152T>C
ENST00000372348.7:c.1142+152T>C	ENSP00000361423.2:n.1142+152T>C
ENST00000318560.5:c.1085+152T>C	ENSP00000323315.5:n.1085+152T>C
ENST00000372348.6:c.1142+152T>C	ENSP00000361423.2:n.1142+152T>C
NM_005157.5:c.1085+152T>C	NP_005148.2:n.1085+152T>C
NM_007313.2:c.1142+152T>C	NP_009297.2:n.1142+152T>C
NM_005157.6:c.1085+152T>C MANE Select	NP_005148.2:n.1085+152T>C
NM_007313.3:c.1142+152T>C	NP_009297.2:n.1142+152T>C