Canonical Allele Identifier: CA6355039
Community Standard Title: NM_014026.6(DCPS):c.550G>A (p.Ala184Thr)
Gene: DCPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126338313G>A , CM000673.2:g.126338313G>A GRCh38
NC_000011.9:g.126208208G>A , CM000673.1:g.126208208G>A GRCh37
NC_000011.8:g.125713418G>A NCBI36
NG_053153.1:g.40013G>A

Transcript Alleles

HGVS Amino-acid Change
NM_014026.6:c.550G>A MANE Select NP_054745.1:p.Ala184Thr
ENST00000263579.5:c.550G>A MANE Select ENSP00000263579.4:p.Ala184Thr
NM_001350236.1:c.571G>A NP_001337165.1:p.Ala191Thr
NM_001350236.2:c.571G>A NP_001337165.1:p.Ala191Thr
NM_014026.4:c.550G>A NP_054745.1:p.Ala184Thr
NM_014026.5:c.550G>A NP_054745.1:p.Ala184Thr
ENST00000263579.4:c.550G>A ENSP00000263579.4:p.Ala184Thr
ENST00000529149.1:n.1900G>A
ENST00000530860.5:n.148-4994G>A
ENST00000648516.1:c.271G>A ENSP00000497684.1:p.Ala91Thr
XM_011542778.1:c.571G>A XP_011541080.1:p.Ala191Thr
XM_011542779.1:c.271G>A XP_011541081.1:p.Ala91Thr
XM_011542780.1:c.271G>A XP_011541082.1:p.Ala91Thr