Canonical Allele Identifier: CA2627714180
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252973G>A , CM000677.2:g.38252973G>A GRCh38
NC_000015.9:g.38545174G>A , CM000677.1:g.38545174G>A GRCh37
NC_000015.8:g.36332466G>A NCBI36
NG_008980.1:g.5123G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-213G>A MANE Select ENSP00000299084.4:n.-213G>A
ENST00000299084.8:c.-213G>A ENSP00000299084.4:n.-213G>A
ENST00000561205.1:n.126G>A
NM_152594.2:c.-213G>A NP_689807.1:n.-213G>A
XM_005254202.2:c.-213G>A XP_005254259.1:n.-213G>A
XM_005254203.3:c.-260G>A XP_005254260.1:n.-260G>A
XM_005254202.3:c.-213G>A XP_005254259.1:n.-213G>A
XR_001751484.1:n.87+594C>T
NM_152594.3:c.-213G>A MANE Select NP_689807.1:n.-213G>A