Canonical Allele Identifier: CA2170765493
Gene: SPRED1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252919C= , CM000677.2:g.38252919C= GRCh38
NC_000015.9:g.38545120C= , CM000677.1:g.38545120C= GRCh37
NC_000015.8:g.36332412C= NCBI36
NG_008980.1:g.5069C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-267C= MANE Select ENSP00000299084.4:n.-267C=
ENST00000299084.8:c.-267C= ENSP00000299084.4:n.-267C=
ENST00000561205.1:n.72C=
NM_152594.2:c.-267C= NP_689807.1:n.-267C=
XM_005254202.2:c.-267C= XP_005254259.1:n.-267C=
XM_005254203.3:c.-314C= XP_005254260.1:n.-314C=
XM_005254202.3:c.-267C= XP_005254259.1:n.-267C=
XR_001751484.1:n.87+648G=
NM_152594.3:c.-267C= MANE Select NP_689807.1:n.-267C=
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