Canonical Allele Identifier: CA1301576168
Community Standard Title: NM_001017920.3(DAPL1):c.208-1768T=
Gene: DAPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.158813937T= , CM000664.2:g.158813937T= GRCh38
NC_000002.11:g.159670449T= , CM000664.1:g.159670449T= GRCh37
NC_000002.10:g.159378695T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001017920.3:c.208-1768T= MANE Select NP_001017920.2:n.208-1768T=
ENST00000309950.8:c.208-1768T= MANE Select ENSP00000309538.4:n.208-1768T=
NM_001017920.2:c.208-1768T= NP_001017920.2:n.208-1768T=
ENST00000309950.7:c.208-1768T= ENSP00000309538.3:n.208-1768T=
ENST00000343761.4:c.133+6822T=
ENST00000409042.5:c.207+6822T= ENSP00000386422.1:n.207+6822T=
ENST00000619477.4:c.207+6822T= ENSP00000479225.1:n.207+6822T=
ENST00000621326.4:c.327-1768T= ENSP00000479872.1:n.327-1768T=
XM_011512167.1:c.207+6822T= XP_011510469.1:n.207+6822T=