Canonical Allele Identifier: CA2170765513
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252939_38252940delinsCA , CM000677.2:g.38252939_38252940delinsCA GRCh38
NC_000015.9:g.38545140_38545141delinsCA , CM000677.1:g.38545140_38545141delinsCA GRCh37
NC_000015.8:g.36332432_36332433delinsCA NCBI36
NG_008980.1:g.5089_5090delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.-247_-246delinsCA MANE Select ENSP00000299084.4:n.-247_-246delinsCA
ENST00000299084.8:c.-247_-246delinsCA ENSP00000299084.4:n.-247_-246delinsCA
ENST00000561205.1:n.92_93delinsCA
NM_152594.2:c.-247_-246delinsCA NP_689807.1:n.-247_-246delinsCA
XM_005254202.2:c.-247_-246delinsCA XP_005254259.1:n.-247_-246delinsCA
XM_005254203.3:c.-294_-293delinsCA XP_005254260.1:n.-294_-293delinsCA
XM_005254202.3:c.-247_-246delinsCA XP_005254259.1:n.-247_-246delinsCA
XR_001751484.1:n.87+627_87+628delinsTG
NM_152594.3:c.-247_-246delinsCA MANE Select NP_689807.1:n.-247_-246delinsCA