Canonical Allele Identifier: CA391933339
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38351156C>A , CM000677.2:g.38351156C>A GRCh38
NC_000015.9:g.38643357C>A , CM000677.1:g.38643357C>A GRCh37
NC_000015.8:g.36430649C>A NCBI36
NG_008980.1:g.103306C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.827C>A MANE Select ENSP00000299084.4:p.Ala276Asp
ENST00000299084.8:c.827C>A ENSP00000299084.4:p.Ala276Asp
NM_152594.2:c.827C>A NP_689807.1:p.Ala276Asp
XM_005254202.2:c.863C>A XP_005254259.1:p.Ala288Asp
XM_005254203.3:c.605C>A XP_005254260.1:p.Ala202Asp
XM_011521288.1:c.764C>A XP_011519590.1:p.Ala255Asp
XM_011521289.1:c.764C>A XP_011519591.1:p.Ala255Asp
XM_011521290.1:c.764C>A XP_011519592.1:p.Ala255Asp
XM_005254202.3:c.863C>A XP_005254259.1:p.Ala288Asp
XM_011521289.3:c.764C>A XP_011519591.1:p.Ala255Asp
NM_152594.3:c.827C>A MANE Select NP_689807.1:p.Ala276Asp