Canonical Allele Identifier: CA2627714204
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252996_38252997dup , CM000677.2:g.38252996_38252997dup GRCh38
NC_000015.9:g.38545197_38545198dup , CM000677.1:g.38545197_38545198dup GRCh37
NC_000015.8:g.36332489_36332490dup NCBI36
NG_008980.1:g.5146_5147dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-190_-189dup MANE Select ENSP00000299084.4:n.-190_-189dup
ENST00000299084.8:c.-190_-189dup ENSP00000299084.4:n.-190_-189dup
ENST00000561205.1:n.149_150dup
NM_152594.2:c.-190_-189dup NP_689807.1:n.-190_-189dup
XM_005254202.2:c.-190_-189dup XP_005254259.1:n.-190_-189dup
XM_005254203.3:c.-237_-236dup XP_005254260.1:n.-237_-236dup
XM_005254202.3:c.-190_-189dup XP_005254259.1:n.-190_-189dup
XR_001751484.1:n.87+574_87+575dup
NM_152594.3:c.-190_-189dup MANE Select NP_689807.1:n.-190_-189dup