Canonical Allele Identifier: CA10641691
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 315764
ClinVar RCV Id: RCV000303004
dbSNP Id: rs79309779

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38354549G>A , CM000677.2:g.38354549G>A GRCh38
NC_000015.9:g.38646750G>A , CM000677.1:g.38646750G>A GRCh37
NC_000015.8:g.36434042G>A NCBI36
NG_008980.1:g.106699G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*2885G>A MANE Select ENSP00000299084.4:n.*2885G>A
ENST00000299084.8:c.*2885G>A ENSP00000299084.4:n.*2885G>A
NM_152594.2:c.*2885G>A NP_689807.1:n.*2885G>A
XM_005254202.2:c.*2885G>A XP_005254259.1:n.*2885G>A
XM_005254203.3:c.*2885G>A XP_005254260.1:n.*2885G>A
XM_011521288.1:c.*2885G>A XP_011519590.1:n.*2885G>A
XM_011521289.1:c.*2885G>A XP_011519591.1:n.*2885G>A
XM_011521290.1:c.*2885G>A XP_011519592.1:n.*2885G>A
XM_005254202.3:c.*2885G>A XP_005254259.1:n.*2885G>A
XM_011521289.3:c.*2885G>A XP_011519591.1:n.*2885G>A
NM_152594.3:c.*2885G>A MANE Select NP_689807.1:n.*2885G>A