Canonical Allele Identifier: CA2170812634

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351249_38351251delinsACT , CM000677.2:g.38351249_38351251delinsACT	GRCh38
NC_000015.9:g.38643450_38643452delinsACT , CM000677.1:g.38643450_38643452delinsACT	GRCh37
NC_000015.8:g.36430742_36430744delinsACT	NCBI36
NG_008980.1:g.103399_103401delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.920_922delinsACT MANE Select	ENSP00000299084.4:p.Asp307=
ENST00000299084.8:c.920_922delinsACT	ENSP00000299084.4:p.Asp307=
NM_152594.2:c.920_922delinsACT	NP_689807.1:p.Asp307=
XM_005254202.2:c.956_958delinsACT	XP_005254259.1:p.Asp319=
XM_005254203.3:c.698_700delinsACT	XP_005254260.1:p.Asp233=
XM_011521288.1:c.857_859delinsACT	XP_011519590.1:p.Asp286=
XM_011521289.1:c.857_859delinsACT	XP_011519591.1:p.Asp286=
XM_011521290.1:c.857_859delinsACT	XP_011519592.1:p.Asp286=
XM_005254202.3:c.956_958delinsACT	XP_005254259.1:p.Asp319=
XM_011521289.3:c.857_859delinsACT	XP_011519591.1:p.Asp286=
NM_152594.3:c.920_922delinsACT MANE Select	NP_689807.1:p.Asp307=