Canonical Allele Identifier: CA723815602

Gene: RFWD3

Linked Data

• dbSNP Id: rs1402030822
• MyVariant Identifiers: chr16:g.74664678del (hg19) ; chr16:g.74630780del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74630781del , CM000678.2:g.74630781del	GRCh38
NC_000016.9:g.74664679del , CM000678.1:g.74664679del	GRCh37
NC_000016.8:g.73222180del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361070.9:c.1754+1del
ENST00000361070.8:c.1754+1del
ENST00000571750.5:c.1754+1del
ENST00000575154.1:n.388+1del
NM_018124.3:c.1754+1del
XM_005256021.3:c.1754+1del
XM_005256022.3:c.1754+1del
XM_006721228.2:c.1577+1743del	XP_006721291.1:n.1577+1743del
XM_011523191.1:c.1754+1del
XM_005256021.4:c.1754+1del
XM_005256022.4:c.1754+1del
XM_006721228.3:c.1577+1743del	XP_006721291.1:n.1577+1743del
XM_011523191.3:c.1754+1del
XM_017023391.1:c.1754+1del
XM_017023392.1:c.1577+1743del	XP_016878881.1:n.1577+1743del
NM_018124.4:c.1754+1del
NM_001370534.1:c.1754+1del
NM_001370535.1:c.1754+1del
NM_001370536.1:c.1577+1743del	NP_001357465.1:n.1577+1743del
NM_001370537.1:c.920+1del
NM_001370539.1:c.920+1del
NM_001370540.1:c.920+1del
NM_001370542.1:c.920+1del
NM_001370543.1:c.920+1del