Canonical Allele Identifier: CA2170811895

Gene: SPRED1

Linked Data

• dbSNP Id: rs1896213547

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349580_38349581insGTAGT , CM000677.2:g.38349580_38349581insGTAGT	GRCh38
NC_000015.9:g.38641781_38641782insGTAGT , CM000677.1:g.38641781_38641782insGTAGT	GRCh37
NC_000015.8:g.36429073_36429074insGTAGT	NCBI36
NG_008980.1:g.101730_101731insGTAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.684+57_684+58insGTAGT MANE Select	ENSP00000299084.4:n.684+57_684+58insGTAGT
ENST00000299084.8:c.684+57_684+58insGTAGT	ENSP00000299084.4:n.684+57_684+58insGTAGT
NM_152594.2:c.684+57_684+58insGTAGT	NP_689807.1:n.684+57_684+58insGTAGT
XM_005254202.2:c.720+57_720+58insGTAGT	XP_005254259.1:n.720+57_720+58insGTAGT
XM_005254203.3:c.462+57_462+58insGTAGT	XP_005254260.1:n.462+57_462+58insGTAGT
XM_011521288.1:c.621+57_621+58insGTAGT	XP_011519590.1:n.621+57_621+58insGTAGT
XM_011521289.1:c.621+57_621+58insGTAGT	XP_011519591.1:n.621+57_621+58insGTAGT
XM_011521290.1:c.621+57_621+58insGTAGT	XP_011519592.1:n.621+57_621+58insGTAGT
XM_005254202.3:c.720+57_720+58insGTAGT	XP_005254259.1:n.720+57_720+58insGTAGT
XM_011521289.3:c.621+57_621+58insGTAGT	XP_011519591.1:n.621+57_621+58insGTAGT
NM_152594.3:c.684+57_684+58insGTAGT MANE Select	NP_689807.1:n.684+57_684+58insGTAGT