Canonical Allele Identifier: CA6354966
Gene: DCPS HGNC NCBI
COSMIC:
COSM3998317 (not active)
gnomAD v2:
11:126201290 A / G
gnomAD v3:
11:126331395 A / G
gnomAD v4:
chr11-126331395-A-G
Joint Max Group AF 0.26744174 (AMR)
Genomes Max Group AF 0.25713804 (AMR)
Exomes Max Group AF 0.26926437 (AMR)
dbSNP:
651922
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126331395A>G , CM000673.2:g.126331395A>G GRCh38
NC_000011.9:g.126201290A>G , CM000673.1:g.126201290A>G GRCh37
NC_000011.8:g.125706500A>G NCBI36
NG_053153.1:g.33095A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263579.5:c.377-10A>G MANE Select ENSP00000263579.4:n.377-10A>G
ENST00000648516.1:c.98-10A>G ENSP00000497684.1:n.98-10A>G
ENST00000263579.4:c.377-10A>G ENSP00000263579.4:n.377-10A>G
NM_014026.4:c.377-10A>G NP_054745.1:n.377-10A>G
XM_011542778.1:c.398-10A>G XP_011541080.1:n.398-10A>G
XM_011542779.1:c.98-10A>G XP_011541081.1:n.98-10A>G
XM_011542780.1:c.98-10A>G XP_011541082.1:n.98-10A>G
NM_001350236.1:c.398-10A>G NP_001337165.1:n.398-10A>G
NM_014026.5:c.377-10A>G NP_054745.1:n.377-10A>G
NM_014026.6:c.377-10A>G MANE Select NP_054745.1:n.377-10A>G
NM_001350236.2:c.398-10A>G NP_001337165.1:n.398-10A>G
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