Canonical Allele Identifier: CA2170765634
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253034C= , CM000677.2:g.38253034C= GRCh38
NC_000015.9:g.38545235C= , CM000677.1:g.38545235C= GRCh37
NC_000015.8:g.36332527C= NCBI36
NG_008980.1:g.5184C=

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.-152C= MANE Select ENSP00000299084.4:n.-152C=
ENST00000299084.8:c.-152C= ENSP00000299084.4:n.-152C=
ENST00000561205.1:n.187C=
NM_152594.2:c.-152C= NP_689807.1:n.-152C=
XM_005254202.2:c.-152C= XP_005254259.1:n.-152C=
XM_005254203.3:c.-199C= XP_005254260.1:n.-199C=
XM_005254202.3:c.-152C= XP_005254259.1:n.-152C=
XR_001751484.1:n.87+533G=
NM_152594.3:c.-152C= MANE Select NP_689807.1:n.-152C=