Canonical Allele Identifier: CA1257216953

Gene: SPRED2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65381266_65381269delinsCCAG , CM000664.2:g.65381266_65381269delinsCCAG	GRCh38
NC_000002.11:g.65608400_65608403delinsCCAG , CM000664.1:g.65608400_65608403delinsCCAG	GRCh37
NC_000002.10:g.65461904_65461907delinsCCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356388.9:c.27-36373_27-36370delinsCTGG MANE Select	ENSP00000348753.4:n.27-36373_27-36370delinsCTGG
ENST00000356388.8:c.27-36373_27-36370delinsCTGG	ENSP00000348753.4:n.27-36373_27-36370delinsCTGG
ENST00000440972.1:c.27-36373_27-36370delinsCTGG	ENSP00000406481.1:n.27-36373_27-36370delinsCTGG
NM_181784.2:c.27-36373_27-36370delinsCTGG	NP_861449.2:n.27-36373_27-36370delinsCTGG
XM_005264200.3:c.27-36373_27-36370delinsCTGG	XP_005264257.2:n.27-36373_27-36370delinsCTGG
XM_005264202.3:c.27-36373_27-36370delinsCTGG	XP_005264259.1:n.27-36373_27-36370delinsCTGG
XM_006711966.1:c.27-36373_27-36370delinsCTGG	XP_006712029.1:n.27-36373_27-36370delinsCTGG
XM_005264200.5:c.27-36373_27-36370delinsCTGG	XP_005264257.2:n.27-36373_27-36370delinsCTGG
XM_005264202.5:c.27-36373_27-36370delinsCTGG	XP_005264259.1:n.27-36373_27-36370delinsCTGG
NM_181784.3:c.27-36373_27-36370delinsCTGG MANE Select	NP_861449.2:n.27-36373_27-36370delinsCTGG