Canonical Allele Identifier: CA2627714272
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253049_38253065dup , CM000677.2:g.38253049_38253065dup GRCh38
NC_000015.9:g.38545250_38545266dup , CM000677.1:g.38545250_38545266dup GRCh37
NC_000015.8:g.36332542_36332558dup NCBI36
NG_008980.1:g.5199_5215dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-137_-121dup MANE Select ENSP00000299084.4:n.-137_-121dup
ENST00000299084.8:c.-137_-121dup ENSP00000299084.4:n.-137_-121dup
ENST00000561205.1:n.202_218dup
NM_152594.2:c.-137_-121dup NP_689807.1:n.-137_-121dup
XM_005254202.2:c.-137_-121dup XP_005254259.1:n.-137_-121dup
XM_005254203.3:c.-184_-168dup XP_005254260.1:n.-184_-168dup
XM_005254202.3:c.-137_-121dup XP_005254259.1:n.-137_-121dup
XR_001751484.1:n.87+510_87+526dup
NM_152594.3:c.-137_-121dup MANE Select NP_689807.1:n.-137_-121dup