Canonical Allele Identifier: CA114319659

Gene: DAP

Linked Data

• dbSNP Id: rs946254917
• gnomAD v3: 5-10733580-T-C
• gnomAD v4: 5-10733580-T-C
• MyVariant Identifiers: chr5:g.10733692T>C (hg19) ; chr5:g.10733580T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10733580T>C , CM000667.2:g.10733580T>C	GRCh38
NC_000005.9:g.10733692T>C , CM000667.1:g.10733692T>C	GRCh37
NC_000005.8:g.10786692T>C	NCBI36
NG_011546.1:g.32696A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230895.11:c.152+14595A>G MANE Select	ENSP00000230895.7:n.152+14595A>G
ENST00000230895.10:c.152+14595A>G	ENSP00000230895.6:n.152+14595A>G
ENST00000432074.2:c.152+14595A>G	ENSP00000394163.2:n.152+14595A>G
ENST00000508253.5:n.309+14595A>G
ENST00000514882.5:n.220+14595A>G
NM_001291963.1:c.152+14595A>G	NP_001278892.1:n.152+14595A>G
NM_004394.2:c.152+14595A>G	NP_004385.1:n.152+14595A>G
NM_001291963.2:c.152+14595A>G	NP_001278892.1:n.152+14595A>G
NM_004394.3:c.152+14595A>G MANE Select	NP_004385.1:n.152+14595A>G