Canonical Allele Identifier: CA2170813116

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38352328_38352333delinsATGATT , CM000677.2:g.38352328_38352333delinsATGATT	GRCh38
NC_000015.9:g.38644529_38644534delinsATGATT , CM000677.1:g.38644529_38644534delinsATGATT	GRCh37
NC_000015.8:g.36431821_36431826delinsATGATT	NCBI36
NG_008980.1:g.104478_104483delinsATGATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*664_*669delinsATGATT MANE Select	ENSP00000299084.4:n.*664_*669delinsATGATT
ENST00000299084.8:c.*664_*669delinsATGATT	ENSP00000299084.4:n.*664_*669delinsATGATT
NM_152594.2:c.*664_*669delinsATGATT	NP_689807.1:n.*664_*669delinsATGATT
XM_005254202.2:c.*664_*669delinsATGATT	XP_005254259.1:n.*664_*669delinsATGATT
XM_005254203.3:c.*664_*669delinsATGATT	XP_005254260.1:n.*664_*669delinsATGATT
XM_011521288.1:c.*664_*669delinsATGATT	XP_011519590.1:n.*664_*669delinsATGATT
XM_011521289.1:c.*664_*669delinsATGATT	XP_011519591.1:n.*664_*669delinsATGATT
XM_011521290.1:c.*664_*669delinsATGATT	XP_011519592.1:n.*664_*669delinsATGATT
XM_005254202.3:c.*664_*669delinsATGATT	XP_005254259.1:n.*664_*669delinsATGATT
XM_011521289.3:c.*664_*669delinsATGATT	XP_011519591.1:n.*664_*669delinsATGATT
NM_152594.3:c.*664_*669delinsATGATT MANE Select	NP_689807.1:n.*664_*669delinsATGATT