Canonical Allele Identifier: CA2170813017

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38352124_38352128delinsATTAG , CM000677.2:g.38352124_38352128delinsATTAG	GRCh38
NC_000015.9:g.38644325_38644329delinsATTAG , CM000677.1:g.38644325_38644329delinsATTAG	GRCh37
NC_000015.8:g.36431617_36431621delinsATTAG	NCBI36
NG_008980.1:g.104274_104278delinsATTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*460_*464delinsATTAG MANE Select	ENSP00000299084.4:n.*460_*464delinsATTAG
ENST00000299084.8:c.*460_*464delinsATTAG	ENSP00000299084.4:n.*460_*464delinsATTAG
NM_152594.2:c.*460_*464delinsATTAG	NP_689807.1:n.*460_*464delinsATTAG
XM_005254202.2:c.*460_*464delinsATTAG	XP_005254259.1:n.*460_*464delinsATTAG
XM_005254203.3:c.*460_*464delinsATTAG	XP_005254260.1:n.*460_*464delinsATTAG
XM_011521288.1:c.*460_*464delinsATTAG	XP_011519590.1:n.*460_*464delinsATTAG
XM_011521289.1:c.*460_*464delinsATTAG	XP_011519591.1:n.*460_*464delinsATTAG
XM_011521290.1:c.*460_*464delinsATTAG	XP_011519592.1:n.*460_*464delinsATTAG
XM_005254202.3:c.*460_*464delinsATTAG	XP_005254259.1:n.*460_*464delinsATTAG
XM_011521289.3:c.*460_*464delinsATTAG	XP_011519591.1:n.*460_*464delinsATTAG
NM_152594.3:c.*460_*464delinsATTAG MANE Select	NP_689807.1:n.*460_*464delinsATTAG