Canonical Allele Identifier: CA1527147688

Gene: DAP

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10695414T= , CM000667.2:g.10695414T=	GRCh38
NC_000005.9:g.10695526T= , CM000667.1:g.10695526T=	GRCh37
NC_000005.8:g.10748526T=	NCBI36
NG_011546.1:g.70862A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230895.11:c.153-11843A= MANE Select	ENSP00000230895.7:n.153-11843A=
ENST00000230895.10:c.153-11843A=	ENSP00000230895.6:n.153-11843A=
ENST00000432074.2:c.153-14245A=	ENSP00000394163.2:n.153-14245A=
ENST00000508253.5:n.310-11843A=
ENST00000514882.5:n.221-11843A=
NM_001291963.1:c.153-14245A=	NP_001278892.1:n.153-14245A=
NM_004394.2:c.153-11843A=	NP_004385.1:n.153-11843A=
NM_001291963.2:c.153-14245A=	NP_001278892.1:n.153-14245A=
NM_004394.3:c.153-11843A= MANE Select	NP_004385.1:n.153-11843A=