Canonical Allele Identifier: CA2627716459
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38352131_38352132insCAC , CM000677.2:g.38352131_38352132insCAC GRCh38
NC_000015.9:g.38644332_38644333insCAC , CM000677.1:g.38644332_38644333insCAC GRCh37
NC_000015.8:g.36431624_36431625insCAC NCBI36
NG_008980.1:g.104281_104282insCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.*467_*468insCAC MANE Select ENSP00000299084.4:n.*467_*468insCAC
ENST00000299084.8:c.*467_*468insCAC ENSP00000299084.4:n.*467_*468insCAC
NM_152594.2:c.*467_*468insCAC NP_689807.1:n.*467_*468insCAC
XM_005254202.2:c.*467_*468insCAC XP_005254259.1:n.*467_*468insCAC
XM_005254203.3:c.*467_*468insCAC XP_005254260.1:n.*467_*468insCAC
XM_011521288.1:c.*467_*468insCAC XP_011519590.1:n.*467_*468insCAC
XM_011521289.1:c.*467_*468insCAC XP_011519591.1:n.*467_*468insCAC
XM_011521290.1:c.*467_*468insCAC XP_011519592.1:n.*467_*468insCAC
XM_005254202.3:c.*467_*468insCAC XP_005254259.1:n.*467_*468insCAC
XM_011521289.3:c.*467_*468insCAC XP_011519591.1:n.*467_*468insCAC
NM_152594.3:c.*467_*468insCAC MANE Select NP_689807.1:n.*467_*468insCAC