Canonical Allele Identifier: CA1257217381

Gene: SPRED2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65381848_65381849delinsTG , CM000664.2:g.65381848_65381849delinsTG	GRCh38
NC_000002.11:g.65608982_65608983delinsTG , CM000664.1:g.65608982_65608983delinsTG	GRCh37
NC_000002.10:g.65462486_65462487delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356388.9:c.27-36953_27-36952delinsCA MANE Select	ENSP00000348753.4:n.27-36953_27-36952delinsCA
ENST00000356388.8:c.27-36953_27-36952delinsCA	ENSP00000348753.4:n.27-36953_27-36952delinsCA
ENST00000440972.1:c.27-36953_27-36952delinsCA	ENSP00000406481.1:n.27-36953_27-36952delinsCA
NM_181784.2:c.27-36953_27-36952delinsCA	NP_861449.2:n.27-36953_27-36952delinsCA
XM_005264200.3:c.27-36953_27-36952delinsCA	XP_005264257.2:n.27-36953_27-36952delinsCA
XM_005264202.3:c.27-36953_27-36952delinsCA	XP_005264259.1:n.27-36953_27-36952delinsCA
XM_006711966.1:c.27-36953_27-36952delinsCA	XP_006712029.1:n.27-36953_27-36952delinsCA
XM_005264200.5:c.27-36953_27-36952delinsCA	XP_005264257.2:n.27-36953_27-36952delinsCA
XM_005264202.5:c.27-36953_27-36952delinsCA	XP_005264259.1:n.27-36953_27-36952delinsCA
NM_181784.3:c.27-36953_27-36952delinsCA MANE Select	NP_861449.2:n.27-36953_27-36952delinsCA