Canonical Allele Identifier: CA2530324270
Gene: SPRED2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.65381789A>G , CM000664.2:g.65381789A>G GRCh38
NC_000002.11:g.65608923A>G , CM000664.1:g.65608923A>G GRCh37
NC_000002.10:g.65462427A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356388.9:c.27-36893T>C MANE Select ENSP00000348753.4:n.27-36893T>C
ENST00000356388.8:c.27-36893T>C ENSP00000348753.4:n.27-36893T>C
ENST00000440972.1:c.27-36893T>C ENSP00000406481.1:n.27-36893T>C
NM_181784.2:c.27-36893T>C NP_861449.2:n.27-36893T>C
XM_005264200.3:c.27-36893T>C XP_005264257.2:n.27-36893T>C
XM_005264202.3:c.27-36893T>C XP_005264259.1:n.27-36893T>C
XM_006711966.1:c.27-36893T>C XP_006712029.1:n.27-36893T>C
XM_005264200.5:c.27-36893T>C XP_005264257.2:n.27-36893T>C
XM_005264202.5:c.27-36893T>C XP_005264259.1:n.27-36893T>C
NM_181784.3:c.27-36893T>C MANE Select NP_861449.2:n.27-36893T>C