Canonical Allele Identifier: CA2627716276
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38351798_38351799insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA , CM000677.2:g.38351798_38351799insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA GRCh38
NC_000015.9:g.38643999_38644000insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA , CM000677.1:g.38643999_38644000insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA GRCh37
NC_000015.8:g.36431291_36431292insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA NCBI36
NG_008980.1:g.103948_103949insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA MANE Select ENSP00000299084.4:n.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGA...
ENST00000299084.8:c.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA ENSP00000299084.4:n.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGA...
NM_152594.2:c.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA NP_689807.1:n.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAA...
XM_005254202.2:c.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA XP_005254259.1:n.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCA...
XM_005254203.3:c.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA XP_005254260.1:n.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCA...
XM_011521288.1:c.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA XP_011519590.1:n.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCA...
XM_011521289.1:c.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA XP_011519591.1:n.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCA...
XM_011521290.1:c.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA XP_011519592.1:n.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCA...
XM_005254202.3:c.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA XP_005254259.1:n.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCA...
XM_011521289.3:c.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA XP_011519591.1:n.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCA...
NM_152594.3:c.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAAAAATCTCCCTCTGAGTCTGACATACAATGATA MANE Select NP_689807.1:n.*134_*135insTGTCGTCGCTAGTGTCACACGAACAGGGATCAGAA...