Canonical Allele Identifier: CA2673254159

Gene: DAP

Linked Data

• gnomAD v4: 5-10733695-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10733695A>T , CM000667.2:g.10733695A>T	GRCh38
NC_000005.9:g.10733807A>T , CM000667.1:g.10733807A>T	GRCh37
NC_000005.8:g.10786807A>T	NCBI36
NG_011546.1:g.32581T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230895.11:c.152+14480T>A MANE Select	ENSP00000230895.7:n.152+14480T>A
ENST00000230895.10:c.152+14480T>A	ENSP00000230895.6:n.152+14480T>A
ENST00000432074.2:c.152+14480T>A	ENSP00000394163.2:n.152+14480T>A
ENST00000508253.5:n.309+14480T>A
ENST00000514882.5:n.220+14480T>A
NM_001291963.1:c.152+14480T>A	NP_001278892.1:n.152+14480T>A
NM_004394.2:c.152+14480T>A	NP_004385.1:n.152+14480T>A
NM_001291963.2:c.152+14480T>A	NP_001278892.1:n.152+14480T>A
NM_004394.3:c.152+14480T>A MANE Select	NP_004385.1:n.152+14480T>A