Canonical Allele Identifier: CA2170765863
Gene: SPRED1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253222G= , CM000677.2:g.38253222G= GRCh38
NC_000015.9:g.38545423G= , CM000677.1:g.38545423G= GRCh37
NC_000015.8:g.36332715G= NCBI36
NG_008980.1:g.5372G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.32+5G= MANE Select ENSP00000299084.4:n.32+5G=
ENST00000299084.8:c.32+5G= ENSP00000299084.4:n.32+5G=
ENST00000561205.1:n.370+5G=
ENST00000561317.1:c.-96+5G= ENSP00000453680.1:n.-96+5G=
NM_152594.2:c.32+5G= NP_689807.1:n.32+5G=
XM_005254202.2:c.32+5G= XP_005254259.1:n.32+5G=
XM_005254203.3:c.-16+5G= XP_005254260.1:n.-16+5G=
XM_005254202.3:c.32+5G= XP_005254259.1:n.32+5G=
XR_001751484.1:n.87+345C=
NM_152594.3:c.32+5G= MANE Select NP_689807.1:n.32+5G=
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