Canonical Allele Identifier: CA2627714295
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253059G>T , CM000677.2:g.38253059G>T GRCh38
NC_000015.9:g.38545260G>T , CM000677.1:g.38545260G>T GRCh37
NC_000015.8:g.36332552G>T NCBI36
NG_008980.1:g.5209G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-127G>T MANE Select ENSP00000299084.4:n.-127G>T
ENST00000299084.8:c.-127G>T ENSP00000299084.4:n.-127G>T
ENST00000561205.1:n.212G>T
NM_152594.2:c.-127G>T NP_689807.1:n.-127G>T
XM_005254202.2:c.-127G>T XP_005254259.1:n.-127G>T
XM_005254203.3:c.-174G>T XP_005254260.1:n.-174G>T
XM_005254202.3:c.-127G>T XP_005254259.1:n.-127G>T
XR_001751484.1:n.87+508C>A
NM_152594.3:c.-127G>T MANE Select NP_689807.1:n.-127G>T