Canonical Allele Identifier: CA2170765791
Gene: SPRED1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253184A= , CM000677.2:g.38253184A= GRCh38
NC_000015.9:g.38545385A= , CM000677.1:g.38545385A= GRCh37
NC_000015.8:g.36332677A= NCBI36
NG_008980.1:g.5334A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-2A= MANE Select ENSP00000299084.4:n.-2A=
ENST00000299084.8:c.-2A= ENSP00000299084.4:n.-2A=
ENST00000561205.1:n.337A=
ENST00000561317.1:c.-129A= ENSP00000453680.1:n.-129A=
NM_152594.2:c.-2A= NP_689807.1:n.-2A=
XM_005254202.2:c.-2A= XP_005254259.1:n.-2A=
XM_005254203.3:c.-49A= XP_005254260.1:n.-49A=
XM_005254202.3:c.-2A= XP_005254259.1:n.-2A=
XR_001751484.1:n.87+383T=
NM_152594.3:c.-2A= MANE Select NP_689807.1:n.-2A=
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