Canonical Allele Identifier: CA391931850
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253214A>C , CM000677.2:g.38253214A>C GRCh38
NC_000015.9:g.38545415A>C , CM000677.1:g.38545415A>C GRCh37
NC_000015.8:g.36332707A>C NCBI36
NG_008980.1:g.5364A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.29A>C MANE Select ENSP00000299084.4:p.Asn10Thr
ENST00000299084.8:c.29A>C ENSP00000299084.4:p.Asn10Thr
ENST00000561205.1:n.367A>C
ENST00000561317.1:c.-99A>C ENSP00000453680.1:n.-99A>C
NM_152594.2:c.29A>C NP_689807.1:p.Asn10Thr
XM_005254202.2:c.29A>C XP_005254259.1:p.Asn10Thr
XM_005254203.3:c.-19A>C XP_005254260.1:n.-19A>C
XM_005254202.3:c.29A>C XP_005254259.1:p.Asn10Thr
XR_001751484.1:n.87+353T>G
NM_152594.3:c.29A>C MANE Select NP_689807.1:p.Asn10Thr