Canonical Allele Identifier: CA13530118
Gene: ELP4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs964112

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.31657400C>A , CM000673.2:g.31657400C>A GRCh38
NC_000011.8:g.31635524C>A NCBI36
NC_000011.9:g.31678948C>A , CM000673.1:g.31678948C>A GRCh37
NG_034086.1:g.152672C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000350638.9:c.1143+7179C>A ENSP00000298937.8:p.=
ENST00000379163.9:c.1146+7179C>A ENSP00000368461.5:p.=
ENST00000395934.2:c.1143+7179C>A ENSP00000379267.2:p.=
NM_001288725.1:c.1146+7179C>A NP_001275654.1:p.=
NM_001288726.1:c.1143+7179C>A NP_001275655.1:p.=
NM_019040.4:c.1143+7179C>A NP_061913.3:p.=
XM_005252865.2:c.1146+7179C>A XP_005252922.1:p.=
XM_011519986.1:c.1146+7179C>A XP_011518288.1:p.=
XM_011519987.1:c.1143+7179C>A XP_011518289.1:p.=
XM_011519988.1:c.1147-5126C>A XP_011518290.1:p.=
XM_011519989.1:c.1146+7179C>A XP_011518291.1:p.=