Canonical Allele Identifier: CA49368894
Gene: SPRED2 HGNC NCBI

Linked Data

dbSNP Id: rs534411376

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.65381891C>A , CM000664.2:g.65381891C>A GRCh38
NC_000002.11:g.65609025C>A , CM000664.1:g.65609025C>A GRCh37
NC_000002.10:g.65462529C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356388.9:c.27-36995G>T MANE Select ENSP00000348753.4:n.27-36995G>T
ENST00000356388.8:c.27-36995G>T ENSP00000348753.4:n.27-36995G>T
ENST00000440972.1:c.27-36995G>T ENSP00000406481.1:n.27-36995G>T
NM_181784.2:c.27-36995G>T NP_861449.2:n.27-36995G>T
XM_005264200.3:c.27-36995G>T XP_005264257.2:n.27-36995G>T
XM_005264202.3:c.27-36995G>T XP_005264259.1:n.27-36995G>T
XM_006711966.1:c.27-36995G>T XP_006712029.1:n.27-36995G>T
XM_005264200.5:c.27-36995G>T XP_005264257.2:n.27-36995G>T
XM_005264202.5:c.27-36995G>T XP_005264259.1:n.27-36995G>T
NM_181784.3:c.27-36995G>T MANE Select NP_861449.2:n.27-36995G>T