Canonical Allele Identifier: CA49358725
Gene: SPRED2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.65368452G>T , CM000664.2:g.65368452G>T GRCh38
NC_000002.11:g.65595586G>T , CM000664.1:g.65595586G>T GRCh37
NC_000002.10:g.65449090G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356388.9:c.27-23556C>A MANE Select ENSP00000348753.4:n.27-23556C>A
ENST00000356388.8:c.27-23556C>A ENSP00000348753.4:n.27-23556C>A
ENST00000440972.1:c.27-23556C>A ENSP00000406481.1:n.27-23556C>A
ENST00000452315.5:c.71+9161C>A ENSP00000390595.1:n.71+9161C>A
NM_181784.2:c.27-23556C>A NP_861449.2:n.27-23556C>A
XM_005264200.3:c.27-23556C>A XP_005264257.2:n.27-23556C>A
XM_005264202.3:c.27-23556C>A XP_005264259.1:n.27-23556C>A
XM_006711966.1:c.27-23556C>A XP_006712029.1:n.27-23556C>A
XM_005264200.5:c.27-23556C>A XP_005264257.2:n.27-23556C>A
XM_005264202.5:c.27-23556C>A XP_005264259.1:n.27-23556C>A
NM_181784.3:c.27-23556C>A MANE Select NP_861449.2:n.27-23556C>A
Search 100 bp 5'
Search 100 bp 3'