Canonical Allele Identifier: CA358846047

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210655A>T (hg19) ; chr4:g.183289502A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289502A>T , CM000666.2:g.183289502A>T	GRCh38
NC_000004.11:g.184210655A>T , CM000666.1:g.184210655A>T	GRCh37
NC_000004.10:g.184447649A>T	NCBI36
NG_051586.1:g.195868A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3251A>T MANE Select	ENSP00000384222.3:p.Asn1084Ile
ENST00000403733.7:c.3251A>T	ENSP00000384222.3:p.Asn1084Ile
ENST00000427431.5:c.*2643A>T	ENSP00000393342.1:n.*2643A>T
ENST00000438543.5:c.*1047A>T	ENSP00000413521.1:n.*1047A>T
ENST00000448232.6:c.3323A>T	ENSP00000398577.2:p.Asn1108Ile
ENST00000504005.5:c.2297A>T	ENSP00000427569.1:p.Asn766Ile
ENST00000508747.1:c.635A>T	ENSP00000420835.1:p.Asn212Ile
ENST00000513834.5:c.3104A>T	ENSP00000425054.1:p.Asn1035Ile
NM_024949.5:c.3251A>T	NP_079225.5:p.Asn1084Ile
XM_011532269.1:c.3323A>T	XP_011530571.1:p.Asn1108Ile
XM_011532269.3:c.3323A>T	XP_011530571.1:p.Asn1108Ile
XM_024454225.1:c.3029A>T	XP_024309993.1:p.Asn1010Ile
NM_024949.6:c.3251A>T MANE Select	NP_079225.5:p.Asn1084Ile