Canonical Allele Identifier: CA15928519

Gene: CABLES1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23155444T>C , CM000680.2:g.23155444T>C	GRCh38
NC_000018.9:g.20735408T>C , CM000680.1:g.20735408T>C	GRCh37
NC_000018.8:g.18989406T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256925.12:c.845+18837T>C MANE Select	ENSP00000256925.7:n.845+18837T>C
ENST00000256925.11:c.845+18837T>C	ENSP00000256925.7:n.845+18837T>C
ENST00000400473.6:c.-137+20774T>C	ENSP00000383321.2:n.-137+20774T>C
ENST00000578052.1:n.59+18837T>C
ENST00000579963.5:c.-137+20793T>C	ENSP00000464435.1:n.-137+20793T>C
ENST00000580153.5:c.-137+18837T>C	ENSP00000461994.1:n.-137+18837T>C
ENST00000580644.5:n.115+18837T>C
ENST00000582882.5:c.184+18837T>C
ENST00000583220.5:n.149+18837T>C
ENST00000585061.1:n.267+5469T>C
NM_001100619.2:c.845+18837T>C	NP_001094089.1:n.845+18837T>C
NM_001256438.1:c.-137+20774T>C	NP_001243367.1:n.-137+20774T>C
NR_023359.1:n.88+20793T>C
NR_023359.2:n.88+20793T>C
NM_001100619.3:c.845+18837T>C MANE Select	NP_001094089.1:n.845+18837T>C