Canonical Allele Identifier: CA7469976
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs746572586

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38299308dup , CM000677.2:g.38299308dup GRCh38
NC_000015.9:g.38591509dup , CM000677.1:g.38591509dup GRCh37
NC_000015.8:g.36378801dup NCBI36
NG_008980.1:g.51458dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.33-65dup MANE Select ENSP00000299084.4:n.33-65dup
ENST00000299084.8:c.33-65dup ENSP00000299084.4:n.33-65dup
ENST00000561205.1:n.371-65dup
ENST00000561317.1:c.-31-65dup ENSP00000453680.1:n.-31-65dup
NM_152594.2:c.33-65dup NP_689807.1:n.33-65dup
XM_005254202.2:c.69-65dup XP_005254259.1:n.69-65dup
XM_005254203.3:c.-15-22933dup XP_005254260.1:n.-15-22933dup
XM_011521288.1:c.-31-65dup XP_011519590.1:n.-31-65dup
XM_011521289.1:c.-31-65dup XP_011519591.1:n.-31-65dup
XM_011521290.1:c.-31-65dup XP_011519592.1:n.-31-65dup
XM_005254202.3:c.69-65dup XP_005254259.1:n.69-65dup
XM_011521289.3:c.-31-65dup XP_011519591.1:n.-31-65dup
NM_152594.3:c.33-65dup MANE Select NP_689807.1:n.33-65dup