Canonical Allele Identifier: CA269293285

Gene: SPRED1

Linked Data

• dbSNP Id: rs67551443
• MyVariant Identifiers: chr15:g.38641776_38641777insT (hg19) ; chr15:g.38349575_38349576insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349575_38349576insT , CM000677.2:g.38349575_38349576insT	GRCh38
NC_000015.9:g.38641776_38641777insT , CM000677.1:g.38641776_38641777insT	GRCh37
NC_000015.8:g.36429068_36429069insT	NCBI36
NG_008980.1:g.101725_101726insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.684+52_684+53insT MANE Select	ENSP00000299084.4:n.684+52_684+53insT
ENST00000299084.8:c.684+52_684+53insT	ENSP00000299084.4:n.684+52_684+53insT
NM_152594.2:c.684+52_684+53insT	NP_689807.1:n.684+52_684+53insT
XM_005254202.2:c.720+52_720+53insT	XP_005254259.1:n.720+52_720+53insT
XM_005254203.3:c.462+52_462+53insT	XP_005254260.1:n.462+52_462+53insT
XM_011521288.1:c.621+52_621+53insT	XP_011519590.1:n.621+52_621+53insT
XM_011521289.1:c.621+52_621+53insT	XP_011519591.1:n.621+52_621+53insT
XM_011521290.1:c.621+52_621+53insT	XP_011519592.1:n.621+52_621+53insT
XM_005254202.3:c.720+52_720+53insT	XP_005254259.1:n.720+52_720+53insT
XM_011521289.3:c.621+52_621+53insT	XP_011519591.1:n.621+52_621+53insT
NM_152594.3:c.684+52_684+53insT MANE Select	NP_689807.1:n.684+52_684+53insT