Canonical Allele Identifier: CA2170813069
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1888506282

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38352242_38352243insGATA , CM000677.2:g.38352242_38352243insGATA GRCh38
NC_000015.9:g.38644443_38644444insGATA , CM000677.1:g.38644443_38644444insGATA GRCh37
NC_000015.8:g.36431735_36431736insGATA NCBI36
NG_008980.1:g.104392_104393insGATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.*578_*579insGATA MANE Select ENSP00000299084.4:n.*578_*579insGATA
ENST00000299084.8:c.*578_*579insGATA ENSP00000299084.4:n.*578_*579insGATA
NM_152594.2:c.*578_*579insGATA NP_689807.1:n.*578_*579insGATA
XM_005254202.2:c.*578_*579insGATA XP_005254259.1:n.*578_*579insGATA
XM_005254203.3:c.*578_*579insGATA XP_005254260.1:n.*578_*579insGATA
XM_011521288.1:c.*578_*579insGATA XP_011519590.1:n.*578_*579insGATA
XM_011521289.1:c.*578_*579insGATA XP_011519591.1:n.*578_*579insGATA
XM_011521290.1:c.*578_*579insGATA XP_011519592.1:n.*578_*579insGATA
XM_005254202.3:c.*578_*579insGATA XP_005254259.1:n.*578_*579insGATA
XM_011521289.3:c.*578_*579insGATA XP_011519591.1:n.*578_*579insGATA
NM_152594.3:c.*578_*579insGATA MANE Select NP_689807.1:n.*578_*579insGATA