Canonical Allele Identifier: CA2170765599
Gene: SPRED1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253017C= , CM000677.2:g.38253017C= GRCh38
NC_000015.9:g.38545218C= , CM000677.1:g.38545218C= GRCh37
NC_000015.8:g.36332510C= NCBI36
NG_008980.1:g.5167C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-169C= MANE Select ENSP00000299084.4:n.-169C=
ENST00000299084.8:c.-169C= ENSP00000299084.4:n.-169C=
ENST00000561205.1:n.170C=
NM_152594.2:c.-169C= NP_689807.1:n.-169C=
XM_005254202.2:c.-169C= XP_005254259.1:n.-169C=
XM_005254203.3:c.-216C= XP_005254260.1:n.-216C=
XM_005254202.3:c.-169C= XP_005254259.1:n.-169C=
XR_001751484.1:n.87+550G=
NM_152594.3:c.-169C= MANE Select NP_689807.1:n.-169C=
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