Canonical Allele Identifier: CA2627714524
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253287A>T , CM000677.2:g.38253287A>T GRCh38
NC_000015.9:g.38545488A>T , CM000677.1:g.38545488A>T GRCh37
NC_000015.8:g.36332780A>T NCBI36
NG_008980.1:g.5437A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.32+70A>T MANE Select ENSP00000299084.4:n.32+70A>T
ENST00000299084.8:c.32+70A>T ENSP00000299084.4:n.32+70A>T
ENST00000561205.1:n.370+70A>T
ENST00000561317.1:c.-96+70A>T ENSP00000453680.1:n.-96+70A>T
NM_152594.2:c.32+70A>T NP_689807.1:n.32+70A>T
XM_005254202.2:c.32+70A>T XP_005254259.1:n.32+70A>T
XM_005254203.3:c.-16+70A>T XP_005254260.1:n.-16+70A>T
XM_005254202.3:c.32+70A>T XP_005254259.1:n.32+70A>T
XR_001751484.1:n.87+280T>A
NM_152594.3:c.32+70A>T MANE Select NP_689807.1:n.32+70A>T