Canonical Allele Identifier: CA771295419

Gene: SPRED2

Linked Data

• dbSNP Id: rs1199584419
• MyVariant Identifiers: chr2:g.65608868_65608869del (hg19) ; chr2:g.65381734_65381735del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65381734_65381735del , CM000664.2:g.65381734_65381735del	GRCh38
NC_000002.11:g.65608868_65608869del , CM000664.1:g.65608868_65608869del	GRCh37
NC_000002.10:g.65462372_65462373del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356388.9:c.27-36839_27-36838del MANE Select	ENSP00000348753.4:n.27-36839_27-36838del
ENST00000356388.8:c.27-36839_27-36838del	ENSP00000348753.4:n.27-36839_27-36838del
ENST00000440972.1:c.27-36839_27-36838del	ENSP00000406481.1:n.27-36839_27-36838del
NM_181784.2:c.27-36839_27-36838del	NP_861449.2:n.27-36839_27-36838del
XM_005264200.3:c.27-36839_27-36838del	XP_005264257.2:n.27-36839_27-36838del
XM_005264202.3:c.27-36839_27-36838del	XP_005264259.1:n.27-36839_27-36838del
XM_006711966.1:c.27-36839_27-36838del	XP_006712029.1:n.27-36839_27-36838del
XM_005264200.5:c.27-36839_27-36838del	XP_005264257.2:n.27-36839_27-36838del
XM_005264202.5:c.27-36839_27-36838del	XP_005264259.1:n.27-36839_27-36838del
NM_181784.3:c.27-36839_27-36838del MANE Select	NP_861449.2:n.27-36839_27-36838del