Canonical Allele Identifier: CA2170765642
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253042G= , CM000677.2:g.38253042G= GRCh38
NC_000015.9:g.38545243G= , CM000677.1:g.38545243G= GRCh37
NC_000015.8:g.36332535G= NCBI36
NG_008980.1:g.5192G=

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.-144G= MANE Select ENSP00000299084.4:n.-144G=
ENST00000299084.8:c.-144G= ENSP00000299084.4:n.-144G=
ENST00000561205.1:n.195G=
NM_152594.2:c.-144G= NP_689807.1:n.-144G=
XM_005254202.2:c.-144G= XP_005254259.1:n.-144G=
XM_005254203.3:c.-191G= XP_005254260.1:n.-191G=
XM_005254202.3:c.-144G= XP_005254259.1:n.-144G=
XR_001751484.1:n.87+525C=
NM_152594.3:c.-144G= MANE Select NP_689807.1:n.-144G=