Canonical Allele Identifier: CA2170788989
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38299414A= , CM000677.2:g.38299414A= GRCh38
NC_000015.9:g.38591615A= , CM000677.1:g.38591615A= GRCh37
NC_000015.8:g.36378907A= NCBI36
NG_008980.1:g.51564A=

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.74A= MANE Select ENSP00000299084.4:p.Asp25=
ENST00000299084.8:c.74A= ENSP00000299084.4:p.Asp25=
ENST00000561205.1:n.412A=
ENST00000561317.1:c.11A= ENSP00000453680.1:p.Asp4=
NM_152594.2:c.74A= NP_689807.1:p.Asp25=
XM_005254202.2:c.110A= XP_005254259.1:p.Asp37=
XM_005254203.3:c.-15-22827A= XP_005254260.1:n.-15-22827A=
XM_011521288.1:c.11A= XP_011519590.1:p.Asp4=
XM_011521289.1:c.11A= XP_011519591.1:p.Asp4=
XM_011521290.1:c.11A= XP_011519592.1:p.Asp4=
XM_005254202.3:c.110A= XP_005254259.1:p.Asp37=
XM_011521289.3:c.11A= XP_011519591.1:p.Asp4=
NM_152594.3:c.74A= MANE Select NP_689807.1:p.Asp25=