Canonical Allele Identifier: CA771295393
Gene: SPRED2 HGNC NCBI

Linked Data

dbSNP Id: rs1426674977
gnomAD v3: 2-65381712-G-GC
gnomAD v4: 2-65381712-G-GC
MyVariant Identifiers: chr2:g.65608846_65608847insC (hg19) chr2:g.65381712_65381713insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.65381715dup , CM000664.2:g.65381715dup GRCh38
NC_000002.11:g.65608849dup , CM000664.1:g.65608849dup GRCh37
NC_000002.10:g.65462353dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356388.9:c.27-36817dup MANE Select ENSP00000348753.4:n.27-36817dup
ENST00000356388.8:c.27-36817dup ENSP00000348753.4:n.27-36817dup
ENST00000440972.1:c.27-36817dup ENSP00000406481.1:n.27-36817dup
NM_181784.2:c.27-36817dup NP_861449.2:n.27-36817dup
XM_005264200.3:c.27-36817dup XP_005264257.2:n.27-36817dup
XM_005264202.3:c.27-36817dup XP_005264259.1:n.27-36817dup
XM_006711966.1:c.27-36817dup XP_006712029.1:n.27-36817dup
XM_005264200.5:c.27-36817dup XP_005264257.2:n.27-36817dup
XM_005264202.5:c.27-36817dup XP_005264259.1:n.27-36817dup
NM_181784.3:c.27-36817dup MANE Select NP_861449.2:n.27-36817dup
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