Canonical Allele Identifier: CA2170799282
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38322171_38322175delinsTTGTA , CM000677.2:g.38322171_38322175delinsTTGTA GRCh38
NC_000015.9:g.38614372_38614376delinsTTGTA , CM000677.1:g.38614372_38614376delinsTTGTA GRCh37
NC_000015.8:g.36401664_36401668delinsTTGTA NCBI36
NG_008980.1:g.74321_74325delinsTTGTA

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.208-70_208-66delinsTTGTA MANE Select ENSP00000299084.4:n.208-70_208-66delinsTT...
ENST00000299084.8:c.208-70_208-66delinsTTGTA ENSP00000299084.4:n.208-70_208-66delinsTT...
ENST00000561205.1:n.546-70_546-66delinsTTGTA
ENST00000561317.1:c.145-70_145-66delinsTTGTA ENSP00000453680.1:n.145-70_145-66delinsTT...
NM_152594.2:c.208-70_208-66delinsTTGTA NP_689807.1:n.208-70_208-66delinsTTGTA
XM_005254202.2:c.244-70_244-66delinsTTGTA XP_005254259.1:n.244-70_244-66delinsTTGTA...
XM_005254203.3:c.-15-70_-15-66delinsTTGTA XP_005254260.1:n.-15-70_-15-66delinsTTGTA...
XM_011521288.1:c.145-70_145-66delinsTTGTA XP_011519590.1:n.145-70_145-66delinsTTGTA...
XM_011521289.1:c.145-70_145-66delinsTTGTA XP_011519591.1:n.145-70_145-66delinsTTGTA...
XM_011521290.1:c.145-70_145-66delinsTTGTA XP_011519592.1:n.145-70_145-66delinsTTGTA...
XM_005254202.3:c.244-70_244-66delinsTTGTA XP_005254259.1:n.244-70_244-66delinsTTGTA...
XM_011521289.3:c.145-70_145-66delinsTTGTA XP_011519591.1:n.145-70_145-66delinsTTGTA...
NM_152594.3:c.208-70_208-66delinsTTGTA MANE Select NP_689807.1:n.208-70_208-66delinsTTGTA