Canonical Allele Identifier: CA2170765716
Gene: SPRED1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253127G= , CM000677.2:g.38253127G= GRCh38
NC_000015.9:g.38545328G= , CM000677.1:g.38545328G= GRCh37
NC_000015.8:g.36332620G= NCBI36
NG_008980.1:g.5277G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-59G= MANE Select ENSP00000299084.4:n.-59G=
ENST00000299084.8:c.-59G= ENSP00000299084.4:n.-59G=
ENST00000561205.1:n.280G=
NM_152594.2:c.-59G= NP_689807.1:n.-59G=
XM_005254202.2:c.-59G= XP_005254259.1:n.-59G=
XM_005254203.3:c.-106G= XP_005254260.1:n.-106G=
XM_005254202.3:c.-59G= XP_005254259.1:n.-59G=
XR_001751484.1:n.87+440C=
NM_152594.3:c.-59G= MANE Select NP_689807.1:n.-59G=
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