Canonical Allele Identifier: CA251951
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1810
dbSNP Id: rs121434313

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38299410C>T , CM000677.2:g.38299410C>T GRCh38
NC_000015.9:g.38591611C>T , CM000677.1:g.38591611C>T GRCh37
NC_000015.8:g.36378903C>T NCBI36
NG_008980.1:g.51560C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.70C>T MANE Select ENSP00000299084.4:p.Arg24Ter
ENST00000299084.8:c.70C>T ENSP00000299084.4:p.Arg24Ter
ENST00000561205.1:n.408C>T
ENST00000561317.1:c.7C>T ENSP00000453680.1:p.Arg3Ter
NM_152594.2:c.70C>T NP_689807.1:p.Arg24Ter
XM_005254202.2:c.106C>T XP_005254259.1:p.Arg36Ter
XM_005254203.3:c.-15-22831C>T XP_005254260.1:n.-15-22831C>T
XM_011521288.1:c.7C>T XP_011519590.1:p.Arg3Ter
XM_011521289.1:c.7C>T XP_011519591.1:p.Arg3Ter
XM_011521290.1:c.7C>T XP_011519592.1:p.Arg3Ter
XM_005254202.3:c.106C>T XP_005254259.1:p.Arg36Ter
XM_011521289.3:c.7C>T XP_011519591.1:p.Arg3Ter
NM_152594.3:c.70C>T MANE Select NP_689807.1:p.Arg24Ter