Canonical Allele Identifier: CA2170812751
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38351531G= , CM000677.2:g.38351531G= GRCh38
NC_000015.9:g.38643732G= , CM000677.1:g.38643732G= GRCh37
NC_000015.8:g.36431024G= NCBI36
NG_008980.1:g.103681G=

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.1202G= MANE Select ENSP00000299084.4:p.Cys401=
ENST00000299084.8:c.1202G= ENSP00000299084.4:p.Cys401=
NM_152594.2:c.1202G= NP_689807.1:p.Cys401=
XM_005254202.2:c.1238G= XP_005254259.1:p.Cys413=
XM_005254203.3:c.980G= XP_005254260.1:p.Cys327=
XM_011521288.1:c.1139G= XP_011519590.1:p.Cys380=
XM_011521289.1:c.1139G= XP_011519591.1:p.Cys380=
XM_011521290.1:c.1139G= XP_011519592.1:p.Cys380=
XM_005254202.3:c.1238G= XP_005254259.1:p.Cys413=
XM_011521289.3:c.1139G= XP_011519591.1:p.Cys380=
NM_152594.3:c.1202G= MANE Select NP_689807.1:p.Cys401=