Canonical Allele Identifier: CA2170765603
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253020G= , CM000677.2:g.38253020G= GRCh38
NC_000015.9:g.38545221G= , CM000677.1:g.38545221G= GRCh37
NC_000015.8:g.36332513G= NCBI36
NG_008980.1:g.5170G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-166G= MANE Select ENSP00000299084.4:n.-166G=
ENST00000299084.8:c.-166G= ENSP00000299084.4:n.-166G=
ENST00000561205.1:n.173G=
NM_152594.2:c.-166G= NP_689807.1:n.-166G=
XM_005254202.2:c.-166G= XP_005254259.1:n.-166G=
XM_005254203.3:c.-213G= XP_005254260.1:n.-213G=
XM_005254202.3:c.-166G= XP_005254259.1:n.-166G=
XR_001751484.1:n.87+547C=
NM_152594.3:c.-166G= MANE Select NP_689807.1:n.-166G=