Canonical Allele Identifier: CA284133315

Gene: WWOX MAF

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79212426G>C , CM000678.2:g.79212426G>C	GRCh38
NC_000016.9:g.79246323G>C , CM000678.1:g.79246323G>C	GRCh37
NC_000016.8:g.77803824G>C	NCBI36
NG_011698.1:g.1117773G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*989G>C (WWOX)	ENSP00000507689.1:n.*989G>C
ENST00000566780.6:c.*630G>C (WWOX) MANE Select	ENSP00000457230.1:n.*630G>C
ENST00000402655.6:c.*292G>C (WWOX)	ENSP00000384238.2:n.*292G>C
ENST00000406884.6:c.*630G>C (WWOX)	ENSP00000384495.2:n.*630G>C
ENST00000539474.6:c.*662G>C (WWOX)	ENSP00000445210.2:n.*662G>C
ENST00000566780.5:c.*630G>C (WWOX)	ENSP00000457230.1:n.*630G>C
NM_001291997.1:c.*630G>C (WWOX)	NP_001278926.1:n.*630G>C
NM_016373.3:c.*630G>C (WWOX)	NP_057457.1:n.*630G>C
XM_011523100.1:c.*630G>C (WWOX)	XP_011521402.1:n.*630G>C
XM_011523103.3:c.*847G>C (WWOX)	XP_011521405.1:n.*847G>C
XM_017023279.1:c.*292G>C (WWOX)	XP_016878768.1:n.*292G>C
XM_024450279.1:c.*504C>G (MAF)	XP_024306047.1:n.*504C>G
XR_001751902.2:n.3706C>G (MAF)
XR_002957802.1:n.3706C>G (MAF)
XR_002957803.1:n.3706C>G (MAF)
XR_002957804.1:n.3706C>G (MAF)
NM_016373.4:c.*630G>C (WWOX) MANE Select	NP_057457.1:n.*630G>C
NM_001291997.2:c.*630G>C (WWOX)	NP_001278926.1:n.*630G>C