Canonical Allele Identifier: CA2232896433

Gene: RFWD3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74630856G= , CM000678.2:g.74630856G=	GRCh38
NC_000016.9:g.74664754G= , CM000678.1:g.74664754G=	GRCh37
NC_000016.8:g.73222255G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361070.9:c.1679C= MANE Select	ENSP00000354361.4:p.Ala560=
ENST00000361070.8:c.1679C=	ENSP00000354361.4:p.Ala560=
ENST00000571750.5:c.1679C=	ENSP00000460049.1:p.Ala560=
ENST00000575154.1:n.313C=
NM_018124.3:c.1679C=	NP_060594.3:p.Ala560=
XM_005256021.3:c.1679C=	XP_005256078.1:p.Ala560=
XM_005256022.3:c.1679C=	XP_005256079.1:p.Ala560=
XM_006721228.2:c.1577+1667C=	XP_006721291.1:n.1577+1667C=
XM_011523191.1:c.1679C=	XP_011521493.1:p.Ala560=
XM_005256021.4:c.1679C=	XP_005256078.1:p.Ala560=
XM_005256022.4:c.1679C=	XP_005256079.1:p.Ala560=
XM_006721228.3:c.1577+1667C=	XP_006721291.1:n.1577+1667C=
XM_011523191.3:c.1679C=	XP_011521493.1:p.Ala560=
XM_017023391.1:c.1679C=	XP_016878880.1:p.Ala560=
XM_017023392.1:c.1577+1667C=	XP_016878881.1:n.1577+1667C=
NM_018124.4:c.1679C= MANE Select	NP_060594.3:p.Ala560=
NM_001370534.1:c.1679C=	NP_001357463.1:p.Ala560=
NM_001370535.1:c.1679C=	NP_001357464.1:p.Ala560=
NM_001370536.1:c.1577+1667C=	NP_001357465.1:n.1577+1667C=
NM_001370537.1:c.845C=	NP_001357466.1:p.Ala282=
NM_001370539.1:c.845C=	NP_001357468.1:p.Ala282=
NM_001370540.1:c.845C=	NP_001357469.1:p.Ala282=
NM_001370542.1:c.845C=	NP_001357471.1:p.Ala282=
NM_001370543.1:c.845C=	NP_001357472.1:p.Ala282=