Canonical Allele Identifier: CA2170812652
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38351296_38351310delinsTCAAAACGAAGAAAA , CM000677.2:g.38351296_38351310delinsTCAAAACGAAGAAAA GRCh38
NC_000015.9:g.38643497_38643511delinsTCAAAACGAAGAAAA , CM000677.1:g.38643497_38643511delinsTCAAAACGAAGAAAA GRCh37
NC_000015.8:g.36430789_36430803delinsTCAAAACGAAGAAAA NCBI36
NG_008980.1:g.103446_103460delinsTCAAAACGAAGAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.967_981delinsTCAAAACGAAGAAAA MANE Select ENSP00000299084.4:p.Ser323=
ENST00000299084.8:c.967_981delinsTCAAAACGAAGAAAA ENSP00000299084.4:p.Ser323=
NM_152594.2:c.967_981delinsTCAAAACGAAGAAAA NP_689807.1:p.Ser323=
XM_005254202.2:c.1003_1017delinsTCAAAACGAAGAAAA XP_005254259.1:p.Ser335=
XM_005254203.3:c.745_759delinsTCAAAACGAAGAAAA XP_005254260.1:p.Ser249=
XM_011521288.1:c.904_918delinsTCAAAACGAAGAAAA XP_011519590.1:p.Ser302=
XM_011521289.1:c.904_918delinsTCAAAACGAAGAAAA XP_011519591.1:p.Ser302=
XM_011521290.1:c.904_918delinsTCAAAACGAAGAAAA XP_011519592.1:p.Ser302=
XM_005254202.3:c.1003_1017delinsTCAAAACGAAGAAAA XP_005254259.1:p.Ser335=
XM_011521289.3:c.904_918delinsTCAAAACGAAGAAAA XP_011519591.1:p.Ser302=
NM_152594.3:c.967_981delinsTCAAAACGAAGAAAA MANE Select NP_689807.1:p.Ser323=