Canonical Allele Identifier: CA1257216992
Gene: SPRED2 HGNC NCBI

Linked Data

dbSNP Id: rs1675369123
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.65381316del , CM000664.2:g.65381316del GRCh38
NC_000002.11:g.65608450del , CM000664.1:g.65608450del GRCh37
NC_000002.10:g.65461954del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356388.9:c.27-36419del MANE Select ENSP00000348753.4:n.27-36419del
ENST00000356388.8:c.27-36419del ENSP00000348753.4:n.27-36419del
ENST00000440972.1:c.27-36419del ENSP00000406481.1:n.27-36419del
NM_181784.2:c.27-36419del NP_861449.2:n.27-36419del
XM_005264200.3:c.27-36419del XP_005264257.2:n.27-36419del
XM_005264202.3:c.27-36419del XP_005264259.1:n.27-36419del
XM_006711966.1:c.27-36419del XP_006712029.1:n.27-36419del
XM_005264200.5:c.27-36419del XP_005264257.2:n.27-36419del
XM_005264202.5:c.27-36419del XP_005264259.1:n.27-36419del
NM_181784.3:c.27-36419del MANE Select NP_861449.2:n.27-36419del
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