Canonical Allele Identifier: CA114319657

Gene: DAP

Linked Data

• dbSNP Id: rs754480957
• gnomAD v3: 5-10733576-C-A
• gnomAD v4: 5-10733576-C-A
• MyVariant Identifiers: chr5:g.10733688C>A (hg19) ; chr5:g.10733576C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10733576C>A , CM000667.2:g.10733576C>A	GRCh38
NC_000005.9:g.10733688C>A , CM000667.1:g.10733688C>A	GRCh37
NC_000005.8:g.10786688C>A	NCBI36
NG_011546.1:g.32700G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230895.11:c.152+14599G>T MANE Select	ENSP00000230895.7:n.152+14599G>T
ENST00000230895.10:c.152+14599G>T	ENSP00000230895.6:n.152+14599G>T
ENST00000432074.2:c.152+14599G>T	ENSP00000394163.2:n.152+14599G>T
ENST00000508253.5:n.309+14599G>T
ENST00000514882.5:n.220+14599G>T
NM_001291963.1:c.152+14599G>T	NP_001278892.1:n.152+14599G>T
NM_004394.2:c.152+14599G>T	NP_004385.1:n.152+14599G>T
NM_001291963.2:c.152+14599G>T	NP_001278892.1:n.152+14599G>T
NM_004394.3:c.152+14599G>T MANE Select	NP_004385.1:n.152+14599G>T