Canonical Allele Identifier: CA1257217301

Gene: SPRED2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65381733_65381735delinsGCA , CM000664.2:g.65381733_65381735delinsGCA	GRCh38
NC_000002.11:g.65608867_65608869delinsGCA , CM000664.1:g.65608867_65608869delinsGCA	GRCh37
NC_000002.10:g.65462371_65462373delinsGCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356388.9:c.27-36839_27-36837delinsTGC MANE Select	ENSP00000348753.4:n.27-36839_27-36837delinsTGC
ENST00000356388.8:c.27-36839_27-36837delinsTGC	ENSP00000348753.4:n.27-36839_27-36837delinsTGC
ENST00000440972.1:c.27-36839_27-36837delinsTGC	ENSP00000406481.1:n.27-36839_27-36837delinsTGC
NM_181784.2:c.27-36839_27-36837delinsTGC	NP_861449.2:n.27-36839_27-36837delinsTGC
XM_005264200.3:c.27-36839_27-36837delinsTGC	XP_005264257.2:n.27-36839_27-36837delinsTGC
XM_005264202.3:c.27-36839_27-36837delinsTGC	XP_005264259.1:n.27-36839_27-36837delinsTGC
XM_006711966.1:c.27-36839_27-36837delinsTGC	XP_006712029.1:n.27-36839_27-36837delinsTGC
XM_005264200.5:c.27-36839_27-36837delinsTGC	XP_005264257.2:n.27-36839_27-36837delinsTGC
XM_005264202.5:c.27-36839_27-36837delinsTGC	XP_005264259.1:n.27-36839_27-36837delinsTGC
NM_181784.3:c.27-36839_27-36837delinsTGC MANE Select	NP_861449.2:n.27-36839_27-36837delinsTGC