Canonical Allele Identifier: CA1527128442

Gene: DAP

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.10733588C= , CM000667.2:g.10733588C=	GRCh38
NC_000005.9:g.10733700C= , CM000667.1:g.10733700C=	GRCh37
NC_000005.8:g.10786700C=	NCBI36
NG_011546.1:g.32688G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230895.11:c.152+14587G= MANE Select	ENSP00000230895.7:n.152+14587G=
ENST00000230895.10:c.152+14587G=	ENSP00000230895.6:n.152+14587G=
ENST00000432074.2:c.152+14587G=	ENSP00000394163.2:n.152+14587G=
ENST00000508253.5:n.309+14587G=
ENST00000514882.5:n.220+14587G=
NM_001291963.1:c.152+14587G=	NP_001278892.1:n.152+14587G=
NM_004394.2:c.152+14587G=	NP_004385.1:n.152+14587G=
NM_001291963.2:c.152+14587G=	NP_001278892.1:n.152+14587G=
NM_004394.3:c.152+14587G= MANE Select	NP_004385.1:n.152+14587G=