Canonical Allele Identifier: CA1257217348

Gene: SPRED2

Linked Data

• dbSNP Id: rs1675379661

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65381802del , CM000664.2:g.65381802del	GRCh38
NC_000002.11:g.65608936del , CM000664.1:g.65608936del	GRCh37
NC_000002.10:g.65462440del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356388.9:c.27-36906del MANE Select	ENSP00000348753.4:n.27-36906del
ENST00000356388.8:c.27-36906del	ENSP00000348753.4:n.27-36906del
ENST00000440972.1:c.27-36906del	ENSP00000406481.1:n.27-36906del
NM_181784.2:c.27-36906del	NP_861449.2:n.27-36906del
XM_005264200.3:c.27-36906del	XP_005264257.2:n.27-36906del
XM_005264202.3:c.27-36906del	XP_005264259.1:n.27-36906del
XM_006711966.1:c.27-36906del	XP_006712029.1:n.27-36906del
XM_005264200.5:c.27-36906del	XP_005264257.2:n.27-36906del
XM_005264202.5:c.27-36906del	XP_005264259.1:n.27-36906del
NM_181784.3:c.27-36906del MANE Select	NP_861449.2:n.27-36906del