Canonical Allele Identifier: CA2627716461
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38352135_38352136insACAAGAAG , CM000677.2:g.38352135_38352136insACAAGAAG GRCh38
NC_000015.9:g.38644336_38644337insACAAGAAG , CM000677.1:g.38644336_38644337insACAAGAAG GRCh37
NC_000015.8:g.36431628_36431629insACAAGAAG NCBI36
NG_008980.1:g.104285_104286insACAAGAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.*471_*472insACAAGAAG MANE Select ENSP00000299084.4:n.*471_*472insACAAGAAG
ENST00000299084.8:c.*471_*472insACAAGAAG ENSP00000299084.4:n.*471_*472insACAAGAAG
NM_152594.2:c.*471_*472insACAAGAAG NP_689807.1:n.*471_*472insACAAGAAG
XM_005254202.2:c.*471_*472insACAAGAAG XP_005254259.1:n.*471_*472insACAAGAAG
XM_005254203.3:c.*471_*472insACAAGAAG XP_005254260.1:n.*471_*472insACAAGAAG
XM_011521288.1:c.*471_*472insACAAGAAG XP_011519590.1:n.*471_*472insACAAGAAG
XM_011521289.1:c.*471_*472insACAAGAAG XP_011519591.1:n.*471_*472insACAAGAAG
XM_011521290.1:c.*471_*472insACAAGAAG XP_011519592.1:n.*471_*472insACAAGAAG
XM_005254202.3:c.*471_*472insACAAGAAG XP_005254259.1:n.*471_*472insACAAGAAG
XM_011521289.3:c.*471_*472insACAAGAAG XP_011519591.1:n.*471_*472insACAAGAAG
NM_152594.3:c.*471_*472insACAAGAAG MANE Select NP_689807.1:n.*471_*472insACAAGAAG