Canonical Allele Identifier: CA1257217349
Gene: SPRED2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.65381805T= , CM000664.2:g.65381805T= GRCh38
NC_000002.11:g.65608939T= , CM000664.1:g.65608939T= GRCh37
NC_000002.10:g.65462443T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356388.9:c.27-36909A= MANE Select ENSP00000348753.4:n.27-36909A=
ENST00000356388.8:c.27-36909A= ENSP00000348753.4:n.27-36909A=
ENST00000440972.1:c.27-36909A= ENSP00000406481.1:n.27-36909A=
NM_181784.2:c.27-36909A= NP_861449.2:n.27-36909A=
XM_005264200.3:c.27-36909A= XP_005264257.2:n.27-36909A=
XM_005264202.3:c.27-36909A= XP_005264259.1:n.27-36909A=
XM_006711966.1:c.27-36909A= XP_006712029.1:n.27-36909A=
XM_005264200.5:c.27-36909A= XP_005264257.2:n.27-36909A=
XM_005264202.5:c.27-36909A= XP_005264259.1:n.27-36909A=
NM_181784.3:c.27-36909A= MANE Select NP_861449.2:n.27-36909A=