Canonical Allele Identifier: CA2170812789
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38351633G= , CM000677.2:g.38351633G= GRCh38
NC_000015.9:g.38643834G= , CM000677.1:g.38643834G= GRCh37
NC_000015.8:g.36431126G= NCBI36
NG_008980.1:g.103783G=

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.1304G= MANE Select ENSP00000299084.4:p.Cys435=
ENST00000299084.8:c.1304G= ENSP00000299084.4:p.Cys435=
NM_152594.2:c.1304G= NP_689807.1:p.Cys435=
XM_005254202.2:c.1340G= XP_005254259.1:p.Cys447=
XM_005254203.3:c.1082G= XP_005254260.1:p.Cys361=
XM_011521288.1:c.1241G= XP_011519590.1:p.Cys414=
XM_011521289.1:c.1241G= XP_011519591.1:p.Cys414=
XM_011521290.1:c.1241G= XP_011519592.1:p.Cys414=
XM_005254202.3:c.1340G= XP_005254259.1:p.Cys447=
XM_011521289.3:c.1241G= XP_011519591.1:p.Cys414=
NM_152594.3:c.1304G= MANE Select NP_689807.1:p.Cys435=