Canonical Allele Identifier: CA6925148

Gene: WASF3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.26685735C>T , CM000675.2:g.26685735C>T	GRCh38
NC_000013.10:g.27259872C>T , CM000675.1:g.27259872C>T	GRCh37
NC_000013.9:g.26157872C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006646.6:c.1399C>T MANE Select	NP_006637.2:p.Arg467Trp
ENST00000335327.6:c.1399C>T MANE Select	ENSP00000335055.5:p.Arg467Trp
NM_001291965.1:c.1390C>T	NP_001278894.1:p.Arg464Trp
NM_006646.5:c.1399C>T	NP_006637.2:p.Arg467Trp
ENST00000335327.5:c.1399C>T	ENSP00000335055.5:p.Arg467Trp
ENST00000361042.8:c.1390C>T	ENSP00000354325.4:p.Arg464Trp
XM_011534889.1:c.1399C>T	XP_011533191.1:p.Arg467Trp
XM_011534889.2:c.1399C>T	XP_011533191.1:p.Arg467Trp
XM_011534890.1:c.1399C>T	XP_011533192.1:p.Arg467Trp
XM_024449315.1:c.1399C>T	XP_024305083.1:p.Arg467Trp
XR_001749798.1:n.615-2152G>A