Canonical Allele Identifier: CA2673254150
Gene: DAP HGNC NCBI

Linked Data

gnomAD v4: 5-10733674-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10733674G>T , CM000667.2:g.10733674G>T GRCh38
NC_000005.9:g.10733786G>T , CM000667.1:g.10733786G>T GRCh37
NC_000005.8:g.10786786G>T NCBI36
NG_011546.1:g.32602C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000230895.11:c.152+14501C>A MANE Select ENSP00000230895.7:n.152+14501C>A
ENST00000230895.10:c.152+14501C>A ENSP00000230895.6:n.152+14501C>A
ENST00000432074.2:c.152+14501C>A ENSP00000394163.2:n.152+14501C>A
ENST00000508253.5:n.309+14501C>A
ENST00000514882.5:n.220+14501C>A
NM_001291963.1:c.152+14501C>A NP_001278892.1:n.152+14501C>A
NM_004394.2:c.152+14501C>A NP_004385.1:n.152+14501C>A
NM_001291963.2:c.152+14501C>A NP_001278892.1:n.152+14501C>A
NM_004394.3:c.152+14501C>A MANE Select NP_004385.1:n.152+14501C>A
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