Canonical Allele Identifier: CA1527128460

Gene: DAP

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10733594G= , CM000667.2:g.10733594G=	GRCh38
NC_000005.9:g.10733706G= , CM000667.1:g.10733706G=	GRCh37
NC_000005.8:g.10786706G=	NCBI36
NG_011546.1:g.32682C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230895.11:c.152+14581C= MANE Select	ENSP00000230895.7:n.152+14581C=
ENST00000230895.10:c.152+14581C=	ENSP00000230895.6:n.152+14581C=
ENST00000432074.2:c.152+14581C=	ENSP00000394163.2:n.152+14581C=
ENST00000508253.5:n.309+14581C=
ENST00000514882.5:n.220+14581C=
NM_001291963.1:c.152+14581C=	NP_001278892.1:n.152+14581C=
NM_004394.2:c.152+14581C=	NP_004385.1:n.152+14581C=
NM_001291963.2:c.152+14581C=	NP_001278892.1:n.152+14581C=
NM_004394.3:c.152+14581C= MANE Select	NP_004385.1:n.152+14581C=