Canonical Allele Identifier: CA1031649861

Gene: SPRED2

Linked Data

• dbSNP Id: rs1675382128
• gnomAD v3: 2-65381900-T-TA
• gnomAD v4: 2-65381900-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65381904dup , CM000664.2:g.65381904dup	GRCh38
NC_000002.11:g.65609038dup , CM000664.1:g.65609038dup	GRCh37
NC_000002.10:g.65462542dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356388.9:c.27-37005dup MANE Select	ENSP00000348753.4:n.27-37005dup
ENST00000356388.8:c.27-37005dup	ENSP00000348753.4:n.27-37005dup
ENST00000440972.1:c.27-37005dup	ENSP00000406481.1:n.27-37005dup
NM_181784.2:c.27-37005dup	NP_861449.2:n.27-37005dup
XM_005264200.3:c.27-37005dup	XP_005264257.2:n.27-37005dup
XM_005264202.3:c.27-37005dup	XP_005264259.1:n.27-37005dup
XM_006711966.1:c.27-37005dup	XP_006712029.1:n.27-37005dup
XM_005264200.5:c.27-37005dup	XP_005264257.2:n.27-37005dup
XM_005264202.5:c.27-37005dup	XP_005264259.1:n.27-37005dup
NM_181784.3:c.27-37005dup MANE Select	NP_861449.2:n.27-37005dup