Canonical Allele Identifier: CA459028482

Gene: DLGAP2

Linked Data

• MyVariant Identifiers: chr8:g.1244303A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1296043A>C , CM000670.2:g.1296043A>C	GRCh38
NC_000008.10:g.1244303A>C , CM000670.1:g.1244303A>C	GRCh37
NC_000008.9:g.1231710A>C	NCBI36
NG_009409.2:g.563325A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000421627.7:c.103+37160A>C	ENSP00000400258.3:n.103+37160A>C
ENST00000637795.2:c.106+37160A>C MANE Select	ENSP00000489774.1:n.106+37160A>C
NR_111948.1:n.3040T>G
XM_011534761.1:c.-135+37160A>C	XP_011533063.1:n.-135+37160A>C
XM_011534762.1:c.-135+37160A>C	XP_011533064.1:n.-135+37160A>C
NM_001346810.1:c.106+37160A>C	NP_001333739.1:n.106+37160A>C
NM_001346810.2:c.106+37160A>C MANE Select	NP_001333739.1:n.106+37160A>C