Canonical Allele Identifier: CA1073203614

Gene: DAP

Linked Data

• dbSNP Id: rs1739527926
• gnomAD v3: 5-10733574-C-T
• gnomAD v4: 5-10733574-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10733574C>T , CM000667.2:g.10733574C>T	GRCh38
NC_000005.9:g.10733686C>T , CM000667.1:g.10733686C>T	GRCh37
NC_000005.8:g.10786686C>T	NCBI36
NG_011546.1:g.32702G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000230895.11:c.152+14601G>A MANE Select	ENSP00000230895.7:n.152+14601G>A
ENST00000230895.10:c.152+14601G>A	ENSP00000230895.6:n.152+14601G>A
ENST00000432074.2:c.152+14601G>A	ENSP00000394163.2:n.152+14601G>A
ENST00000508253.5:n.309+14601G>A
ENST00000514882.5:n.220+14601G>A
NM_001291963.1:c.152+14601G>A	NP_001278892.1:n.152+14601G>A
NM_004394.2:c.152+14601G>A	NP_004385.1:n.152+14601G>A
NM_001291963.2:c.152+14601G>A	NP_001278892.1:n.152+14601G>A
NM_004394.3:c.152+14601G>A MANE Select	NP_004385.1:n.152+14601G>A