Canonical Allele Identifier: CA2170765870
Gene: SPRED1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253225C= , CM000677.2:g.38253225C= GRCh38
NC_000015.9:g.38545426C= , CM000677.1:g.38545426C= GRCh37
NC_000015.8:g.36332718C= NCBI36
NG_008980.1:g.5375C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.32+8C= MANE Select ENSP00000299084.4:n.32+8C=
ENST00000299084.8:c.32+8C= ENSP00000299084.4:n.32+8C=
ENST00000561205.1:n.370+8C=
ENST00000561317.1:c.-96+8C= ENSP00000453680.1:n.-96+8C=
NM_152594.2:c.32+8C= NP_689807.1:n.32+8C=
XM_005254202.2:c.32+8C= XP_005254259.1:n.32+8C=
XM_005254203.3:c.-16+8C= XP_005254260.1:n.-16+8C=
XM_005254202.3:c.32+8C= XP_005254259.1:n.32+8C=
XR_001751484.1:n.87+342G=
NM_152594.3:c.32+8C= MANE Select NP_689807.1:n.32+8C=
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