Canonical Allele Identifier: CA391933405
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38351186A>C , CM000677.2:g.38351186A>C GRCh38
NC_000015.9:g.38643387A>C , CM000677.1:g.38643387A>C GRCh37
NC_000015.8:g.36430679A>C NCBI36
NG_008980.1:g.103336A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.857A>C MANE Select ENSP00000299084.4:p.Asp286Ala
ENST00000299084.8:c.857A>C ENSP00000299084.4:p.Asp286Ala
NM_152594.2:c.857A>C NP_689807.1:p.Asp286Ala
XM_005254202.2:c.893A>C XP_005254259.1:p.Asp298Ala
XM_005254203.3:c.635A>C XP_005254260.1:p.Asp212Ala
XM_011521288.1:c.794A>C XP_011519590.1:p.Asp265Ala
XM_011521289.1:c.794A>C XP_011519591.1:p.Asp265Ala
XM_011521290.1:c.794A>C XP_011519592.1:p.Asp265Ala
XM_005254202.3:c.893A>C XP_005254259.1:p.Asp298Ala
XM_011521289.3:c.794A>C XP_011519591.1:p.Asp265Ala
NM_152594.3:c.857A>C MANE Select NP_689807.1:p.Asp286Ala