Canonical Allele Identifier: CA2627714250
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253029_38253030dup , CM000677.2:g.38253029_38253030dup GRCh38
NC_000015.9:g.38545230_38545231dup , CM000677.1:g.38545230_38545231dup GRCh37
NC_000015.8:g.36332522_36332523dup NCBI36
NG_008980.1:g.5179_5180dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-157_-156dup MANE Select ENSP00000299084.4:n.-157_-156dup
ENST00000299084.8:c.-157_-156dup ENSP00000299084.4:n.-157_-156dup
ENST00000561205.1:n.182_183dup
NM_152594.2:c.-157_-156dup NP_689807.1:n.-157_-156dup
XM_005254202.2:c.-157_-156dup XP_005254259.1:n.-157_-156dup
XM_005254203.3:c.-204_-203dup XP_005254260.1:n.-204_-203dup
XM_005254202.3:c.-157_-156dup XP_005254259.1:n.-157_-156dup
XR_001751484.1:n.87+542_87+543dup
NM_152594.3:c.-157_-156dup MANE Select NP_689807.1:n.-157_-156dup