Canonical Allele Identifier: CA658761259

Gene: SPRED1

Linked Data

• PubMed: PMID:19920235

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351533_38351536dup , CM000677.2:g.38351533_38351536dup	GRCh38
NC_000015.9:g.38643734_38643737dup , CM000677.1:g.38643734_38643737dup	GRCh37
NC_000015.8:g.36431026_36431029dup	NCBI36
NG_008980.1:g.103683_103686dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.1204_1207dup MANE Select	ENSP00000299084.4:p.Arg403LeufsTer30
ENST00000299084.8:c.1204_1207dup	ENSP00000299084.4:p.Arg403LeufsTer30
NM_152594.2:c.1204_1207dup	NP_689807.1:p.Arg403LeufsTer30
XM_005254202.2:c.1240_1243dup	XP_005254259.1:p.Arg415LeufsTer30
XM_005254203.3:c.982_985dup	XP_005254260.1:p.Arg329LeufsTer30
XM_011521288.1:c.1141_1144dup	XP_011519590.1:p.Arg382LeufsTer30
XM_011521289.1:c.1141_1144dup	XP_011519591.1:p.Arg382LeufsTer30
XM_011521290.1:c.1141_1144dup	XP_011519592.1:p.Arg382LeufsTer30
XM_005254202.3:c.1240_1243dup	XP_005254259.1:p.Arg415LeufsTer30
XM_011521289.3:c.1141_1144dup	XP_011519591.1:p.Arg382LeufsTer30
NM_152594.3:c.1204_1207dup MANE Select	NP_689807.1:p.Arg403LeufsTer30