Canonical Allele Identifier: CA1031649699

Gene: SPRED2

Linked Data

• dbSNP Id: rs1675369003
• gnomAD v3: 2-65381311-CGG-C
• gnomAD v4: 2-65381311-CGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65381312_65381313del , CM000664.2:g.65381312_65381313del	GRCh38
NC_000002.11:g.65608446_65608447del , CM000664.1:g.65608446_65608447del	GRCh37
NC_000002.10:g.65461950_65461951del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356388.9:c.27-36417_27-36416del MANE Select	ENSP00000348753.4:n.27-36417_27-36416del
ENST00000356388.8:c.27-36417_27-36416del	ENSP00000348753.4:n.27-36417_27-36416del
ENST00000440972.1:c.27-36417_27-36416del	ENSP00000406481.1:n.27-36417_27-36416del
NM_181784.2:c.27-36417_27-36416del	NP_861449.2:n.27-36417_27-36416del
XM_005264200.3:c.27-36417_27-36416del	XP_005264257.2:n.27-36417_27-36416del
XM_005264202.3:c.27-36417_27-36416del	XP_005264259.1:n.27-36417_27-36416del
XM_006711966.1:c.27-36417_27-36416del	XP_006712029.1:n.27-36417_27-36416del
XM_005264200.5:c.27-36417_27-36416del	XP_005264257.2:n.27-36417_27-36416del
XM_005264202.5:c.27-36417_27-36416del	XP_005264259.1:n.27-36417_27-36416del
NM_181784.3:c.27-36417_27-36416del MANE Select	NP_861449.2:n.27-36417_27-36416del