Canonical Allele Identifier: CA1073203619
Gene: DAP HGNC NCBI

Linked Data

dbSNP Id: rs1739528327
gnomAD v3: 5-10733589-A-C
gnomAD v4: 5-10733589-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10733589A>C , CM000667.2:g.10733589A>C GRCh38
NC_000005.9:g.10733701A>C , CM000667.1:g.10733701A>C GRCh37
NC_000005.8:g.10786701A>C NCBI36
NG_011546.1:g.32687T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000230895.11:c.152+14586T>G MANE Select ENSP00000230895.7:n.152+14586T>G
ENST00000230895.10:c.152+14586T>G ENSP00000230895.6:n.152+14586T>G
ENST00000432074.2:c.152+14586T>G ENSP00000394163.2:n.152+14586T>G
ENST00000508253.5:n.309+14586T>G
ENST00000514882.5:n.220+14586T>G
NM_001291963.1:c.152+14586T>G NP_001278892.1:n.152+14586T>G
NM_004394.2:c.152+14586T>G NP_004385.1:n.152+14586T>G
NM_001291963.2:c.152+14586T>G NP_001278892.1:n.152+14586T>G
NM_004394.3:c.152+14586T>G MANE Select NP_004385.1:n.152+14586T>G
Search 100 bp 5'
Search 100 bp 3'