Canonical Allele Identifier: CA658761258

Gene: SPRED1

Linked Data

• PubMed: PMID:24334617

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351484del , CM000677.2:g.38351484del	GRCh38
NC_000015.9:g.38643685del , CM000677.1:g.38643685del	GRCh37
NC_000015.8:g.36430977del	NCBI36
NG_008980.1:g.103634del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1155del MANE Select	ENSP00000299084.4:p.Asp386IlefsTer20
ENST00000299084.8:c.1155del	ENSP00000299084.4:p.Asp386IlefsTer20
NM_152594.2:c.1155del	NP_689807.1:p.Asp386IlefsTer20
XM_005254202.2:c.1191del	XP_005254259.1:p.Asp398IlefsTer20
XM_005254203.3:c.933del	XP_005254260.1:p.Asp312IlefsTer20
XM_011521288.1:c.1092del	XP_011519590.1:p.Asp365IlefsTer20
XM_011521289.1:c.1092del	XP_011519591.1:p.Asp365IlefsTer20
XM_011521290.1:c.1092del	XP_011519592.1:p.Asp365IlefsTer20
XM_005254202.3:c.1191del	XP_005254259.1:p.Asp398IlefsTer20
XM_011521289.3:c.1092del	XP_011519591.1:p.Asp365IlefsTer20
NM_152594.3:c.1155del MANE Select	NP_689807.1:p.Asp386IlefsTer20