Canonical Allele Identifier: CA2627714221
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253005dup , CM000677.2:g.38253005dup GRCh38
NC_000015.9:g.38545206dup , CM000677.1:g.38545206dup GRCh37
NC_000015.8:g.36332498dup NCBI36
NG_008980.1:g.5155dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-181dup MANE Select ENSP00000299084.4:n.-181dup
ENST00000299084.8:c.-181dup ENSP00000299084.4:n.-181dup
ENST00000561205.1:n.158dup
NM_152594.2:c.-181dup NP_689807.1:n.-181dup
XM_005254202.2:c.-181dup XP_005254259.1:n.-181dup
XM_005254203.3:c.-228dup XP_005254260.1:n.-228dup
XM_005254202.3:c.-181dup XP_005254259.1:n.-181dup
XR_001751484.1:n.87+566dup
NM_152594.3:c.-181dup MANE Select NP_689807.1:n.-181dup