Canonical Allele Identifier: CA391933408
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38351187C>A , CM000677.2:g.38351187C>A GRCh38
NC_000015.9:g.38643388C>A , CM000677.1:g.38643388C>A GRCh37
NC_000015.8:g.36430680C>A NCBI36
NG_008980.1:g.103337C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.858C>A MANE Select ENSP00000299084.4:p.Asp286Glu
ENST00000299084.8:c.858C>A ENSP00000299084.4:p.Asp286Glu
NM_152594.2:c.858C>A NP_689807.1:p.Asp286Glu
XM_005254202.2:c.894C>A XP_005254259.1:p.Asp298Glu
XM_005254203.3:c.636C>A XP_005254260.1:p.Asp212Glu
XM_011521288.1:c.795C>A XP_011519590.1:p.Asp265Glu
XM_011521289.1:c.795C>A XP_011519591.1:p.Asp265Glu
XM_011521290.1:c.795C>A XP_011519592.1:p.Asp265Glu
XM_005254202.3:c.894C>A XP_005254259.1:p.Asp298Glu
XM_011521289.3:c.795C>A XP_011519591.1:p.Asp265Glu
NM_152594.3:c.858C>A MANE Select NP_689807.1:p.Asp286Glu