Canonical Allele Identifier: CA1527147689

Gene: DAP

Genomic Alleles

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

Transcript Alleles

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