Canonical Allele Identifier: CA2170812750
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1888488700

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38351523dup , CM000677.2:g.38351523dup GRCh38
NC_000015.9:g.38643724dup , CM000677.1:g.38643724dup GRCh37
NC_000015.8:g.36431016dup NCBI36
NG_008980.1:g.103673dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.1194dup MANE Select ENSP00000299084.4:p.Lys399GlnfsTer?
ENST00000299084.8:c.1194dup ENSP00000299084.4:p.Lys399GlnfsTer?
NM_152594.2:c.1194dup NP_689807.1:p.Lys399GlnfsTer?
XM_005254202.2:c.1230dup XP_005254259.1:p.Lys411GlnfsTer?
XM_005254203.3:c.972dup XP_005254260.1:p.Lys325GlnfsTer?
XM_011521288.1:c.1131dup XP_011519590.1:p.Lys378GlnfsTer?
XM_011521289.1:c.1131dup XP_011519591.1:p.Lys378GlnfsTer?
XM_011521290.1:c.1131dup XP_011519592.1:p.Lys378GlnfsTer?
XM_005254202.3:c.1230dup XP_005254259.1:p.Lys411GlnfsTer?
XM_011521289.3:c.1131dup XP_011519591.1:p.Lys378GlnfsTer?
NM_152594.3:c.1194dup MANE Select NP_689807.1:p.Lys399GlnfsTer?