Canonical Allele Identifier: CA2627716464
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38352141_38352142insACAAGT , CM000677.2:g.38352141_38352142insACAAGT GRCh38
NC_000015.9:g.38644342_38644343insACAAGT , CM000677.1:g.38644342_38644343insACAAGT GRCh37
NC_000015.8:g.36431634_36431635insACAAGT NCBI36
NG_008980.1:g.104291_104292insACAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.*477_*478insACAAGT MANE Select ENSP00000299084.4:n.*477_*478insACAAGT
ENST00000299084.8:c.*477_*478insACAAGT ENSP00000299084.4:n.*477_*478insACAAGT
NM_152594.2:c.*477_*478insACAAGT NP_689807.1:n.*477_*478insACAAGT
XM_005254202.2:c.*477_*478insACAAGT XP_005254259.1:n.*477_*478insACAAGT
XM_005254203.3:c.*477_*478insACAAGT XP_005254260.1:n.*477_*478insACAAGT
XM_011521288.1:c.*477_*478insACAAGT XP_011519590.1:n.*477_*478insACAAGT
XM_011521289.1:c.*477_*478insACAAGT XP_011519591.1:n.*477_*478insACAAGT
XM_011521290.1:c.*477_*478insACAAGT XP_011519592.1:n.*477_*478insACAAGT
XM_005254202.3:c.*477_*478insACAAGT XP_005254259.1:n.*477_*478insACAAGT
XM_011521289.3:c.*477_*478insACAAGT XP_011519591.1:n.*477_*478insACAAGT
NM_152594.3:c.*477_*478insACAAGT MANE Select NP_689807.1:n.*477_*478insACAAGT