Canonical Allele Identifier: CA2170765666
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253074C= , CM000677.2:g.38253074C= GRCh38
NC_000015.9:g.38545275C= , CM000677.1:g.38545275C= GRCh37
NC_000015.8:g.36332567C= NCBI36
NG_008980.1:g.5224C=

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.-112C= MANE Select ENSP00000299084.4:n.-112C=
ENST00000299084.8:c.-112C= ENSP00000299084.4:n.-112C=
ENST00000561205.1:n.227C=
NM_152594.2:c.-112C= NP_689807.1:n.-112C=
XM_005254202.2:c.-112C= XP_005254259.1:n.-112C=
XM_005254203.3:c.-159C= XP_005254260.1:n.-159C=
XM_005254202.3:c.-112C= XP_005254259.1:n.-112C=
XR_001751484.1:n.87+493G=
NM_152594.3:c.-112C= MANE Select NP_689807.1:n.-112C=