Canonical Allele Identifier: CA459028724

Gene: DLGAP2

Linked Data

• MyVariant Identifiers: chr8:g.1244393T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.1296133T>C , CM000670.2:g.1296133T>C	GRCh38
NC_000008.10:g.1244393T>C , CM000670.1:g.1244393T>C	GRCh37
NC_000008.9:g.1231800T>C	NCBI36
NG_009409.2:g.563415T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421627.7:c.103+37250T>C	ENSP00000400258.3:n.103+37250T>C
ENST00000637795.2:c.106+37250T>C MANE Select	ENSP00000489774.1:n.106+37250T>C
NR_111948.1:n.2950A>G
XM_011534761.1:c.-135+37250T>C	XP_011533063.1:n.-135+37250T>C
XM_011534762.1:c.-135+37250T>C	XP_011533064.1:n.-135+37250T>C
NM_001346810.1:c.106+37250T>C	NP_001333739.1:n.106+37250T>C
NM_001346810.2:c.106+37250T>C MANE Select	NP_001333739.1:n.106+37250T>C