Canonical Allele Identifier: CA6099869

Gene: SCYL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65536315G>A , CM000673.2:g.65536315G>A	GRCh38
NC_000011.9:g.65303786G>A , CM000673.1:g.65303786G>A	GRCh37
NC_000011.8:g.65060362G>A	NCBI36
NG_047172.1:g.16251G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020680.4:c.1632G>A MANE Select	NP_065731.3:p.Pro544=
ENST00000270176.10:c.1632G>A MANE Select	ENSP00000270176.5:p.Pro544=
NM_001048218.1:c.1632G>A	NP_001041683.1:p.Pro544=
NM_001048218.2:c.1632G>A	NP_001041683.1:p.Pro544=
NM_020680.3:c.1632G>A	NP_065731.3:p.Pro544=
ENST00000270176.9:c.1632G>A	ENSP00000270176.5:p.Pro544=
ENST00000279270.10:c.564G>A	ENSP00000279270.7:p.Pro188=
ENST00000420247.6:c.1632G>A	ENSP00000408192.2:p.Pro544=
ENST00000524897.5:n.498G>A
ENST00000524944.5:c.1632G>A	ENSP00000432175.1:p.Pro544=
ENST00000525364.5:c.1632G>A	ENSP00000431635.1:p.Pro544=
ENST00000526454.1:n.865G>A
ENST00000527009.5:c.1203G>A	ENSP00000436993.1:p.Pro401=
ENST00000528545.1:c.51G>A	ENSP00000433604.1:p.Pro17=
ENST00000529981.1:n.437G>A
ENST00000531601.1:c.460G>A
ENST00000533862.5:c.1632G>A	ENSP00000437254.1:p.Pro544=
XM_005274118.2:c.1632G>A	XP_005274175.1:p.Pro544=
XM_005274118.4:c.1632G>A	XP_005274175.1:p.Pro544=
XM_005274120.2:c.1632G>A	XP_005274177.1:p.Pro544=
XM_005274120.4:c.1632G>A	XP_005274177.1:p.Pro544=
XM_005274121.2:c.1632G>A	XP_005274178.1:p.Pro544=
XM_005274121.4:c.1632G>A	XP_005274178.1:p.Pro544=
XM_017018030.2:c.1632G>A	XP_016873519.1:p.Pro544=
XM_017018031.2:c.1632G>A	XP_016873520.1:p.Pro544=
XM_017018033.1:c.1203G>A	XP_016873522.1:p.Pro401=
XM_024448619.1:c.1749G>A	XP_024304387.1:p.Pro583=
XM_024448620.1:c.1320G>A	XP_024304388.1:p.Pro440=