Canonical Allele Identifier: CA1757361118
Gene: DLGAP2 HGNC NCBI

Linked Data

dbSNP Id: rs1800164018

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1296022T>A , CM000670.2:g.1296022T>A GRCh38
NC_000008.10:g.1244282T>A , CM000670.1:g.1244282T>A GRCh37
NC_000008.9:g.1231689T>A NCBI36
NG_009409.2:g.563304T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000421627.7:c.103+37139T>A ENSP00000400258.3:n.103+37139T>A
ENST00000637795.2:c.106+37139T>A MANE Select ENSP00000489774.1:n.106+37139T>A
XM_011534761.1:c.-135+37139T>A XP_011533063.1:n.-135+37139T>A
XM_011534762.1:c.-135+37139T>A XP_011533064.1:n.-135+37139T>A
NM_001346810.1:c.106+37139T>A NP_001333739.1:n.106+37139T>A
NM_001346810.2:c.106+37139T>A MANE Select NP_001333739.1:n.106+37139T>A