Canonical Allele Identifier: CA2627714185
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252976_38252996dup , CM000677.2:g.38252976_38252996dup GRCh38
NC_000015.9:g.38545177_38545197dup , CM000677.1:g.38545177_38545197dup GRCh37
NC_000015.8:g.36332469_36332489dup NCBI36
NG_008980.1:g.5126_5146dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-210_-190dup MANE Select ENSP00000299084.4:n.-210_-190dup
ENST00000299084.8:c.-210_-190dup ENSP00000299084.4:n.-210_-190dup
ENST00000561205.1:n.129_149dup
NM_152594.2:c.-210_-190dup NP_689807.1:n.-210_-190dup
XM_005254202.2:c.-210_-190dup XP_005254259.1:n.-210_-190dup
XM_005254203.3:c.-257_-237dup XP_005254260.1:n.-257_-237dup
XM_005254202.3:c.-210_-190dup XP_005254259.1:n.-210_-190dup
XR_001751484.1:n.87+571_87+591dup
NM_152594.3:c.-210_-190dup MANE Select NP_689807.1:n.-210_-190dup