Canonical Allele Identifier: CA1140204961

Gene: SCYL3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169878005C= , CM000663.2:g.169878005C=	GRCh38
NC_000001.10:g.169847146C= , CM000663.1:g.169847146C=	GRCh37
NC_000001.9:g.168113770C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020423.7:c.351+629G= MANE Select	NP_065156.5:n.351+629G=
ENST00000367771.11:c.351+629G= MANE Select	ENSP00000356745.5:n.351+629G=
NM_020423.6:c.351+629G=	NP_065156.5:n.351+629G=
NM_181093.3:c.351+629G=	NP_851607.2:n.351+629G=
NM_181093.4:c.351+629G=	NP_851607.2:n.351+629G=
ENST00000367770.5:c.351+629G=	ENSP00000356744.1:n.351+629G=
ENST00000367771.10:c.351+629G=	ENSP00000356745.5:n.351+629G=
ENST00000367772.8:c.351+629G=	ENSP00000356746.4:n.351+629G=
ENST00000423670.1:c.351+629G=	ENSP00000407993.1:n.351+629G=
ENST00000470238.1:n.566+629G=
XM_006711465.1:c.351+629G=	XP_006711528.1:n.351+629G=
XM_006711467.2:c.351+629G=	XP_006711530.1:n.351+629G=
XM_011509801.1:c.351+629G=	XP_011508103.1:n.351+629G=
XM_011509802.1:c.-76+629G=	XP_011508104.1:n.-76+629G=
XM_011509803.1:c.-76+629G=	XP_011508105.1:n.-76+629G=
XM_017001862.1:c.351+629G=	XP_016857351.1:n.351+629G=
XM_017001863.1:c.351+629G=	XP_016857352.1:n.351+629G=
XM_017001864.1:c.-76+629G=	XP_016857353.1:n.-76+629G=
XM_017001865.1:c.-76+629G=	XP_016857354.1:n.-76+629G=
XM_024448565.1:c.-801+629G=	XP_024304333.1:n.-801+629G=
XR_001737335.2:n.549+629G=
XR_001737336.2:n.549+629G=