Canonical Allele Identifier: CA771295514

Gene: SPRED2

Linked Data

• dbSNP Id: rs1452905196
• gnomAD v3: 2-65381878-C-T
• gnomAD v4: 2-65381878-C-T
• MyVariant Identifiers: chr2:g.65609012C>T (hg19) ; chr2:g.65381878C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65381878C>T , CM000664.2:g.65381878C>T	GRCh38
NC_000002.11:g.65609012C>T , CM000664.1:g.65609012C>T	GRCh37
NC_000002.10:g.65462516C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356388.9:c.27-36982G>A MANE Select	ENSP00000348753.4:n.27-36982G>A
ENST00000356388.8:c.27-36982G>A	ENSP00000348753.4:n.27-36982G>A
ENST00000440972.1:c.27-36982G>A	ENSP00000406481.1:n.27-36982G>A
NM_181784.2:c.27-36982G>A	NP_861449.2:n.27-36982G>A
XM_005264200.3:c.27-36982G>A	XP_005264257.2:n.27-36982G>A
XM_005264202.3:c.27-36982G>A	XP_005264259.1:n.27-36982G>A
XM_006711966.1:c.27-36982G>A	XP_006712029.1:n.27-36982G>A
XM_005264200.5:c.27-36982G>A	XP_005264257.2:n.27-36982G>A
XM_005264202.5:c.27-36982G>A	XP_005264259.1:n.27-36982G>A
NM_181784.3:c.27-36982G>A MANE Select	NP_861449.2:n.27-36982G>A