Canonical Allele Identifier: CA2170765562
Gene: SPRED1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252986C= , CM000677.2:g.38252986C= GRCh38
NC_000015.9:g.38545187C= , CM000677.1:g.38545187C= GRCh37
NC_000015.8:g.36332479C= NCBI36
NG_008980.1:g.5136C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-200C= MANE Select ENSP00000299084.4:n.-200C=
ENST00000299084.8:c.-200C= ENSP00000299084.4:n.-200C=
ENST00000561205.1:n.139C=
NM_152594.2:c.-200C= NP_689807.1:n.-200C=
XM_005254202.2:c.-200C= XP_005254259.1:n.-200C=
XM_005254203.3:c.-247C= XP_005254260.1:n.-247C=
XM_005254202.3:c.-200C= XP_005254259.1:n.-200C=
XR_001751484.1:n.87+581G=
NM_152594.3:c.-200C= MANE Select NP_689807.1:n.-200C=
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