Canonical Allele Identifier: CA8876744

Gene: DLGAP1 DLGAP1-AS3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.3879648G>A , CM000680.2:g.3879648G>A	GRCh38
NC_000018.9:g.3879648G>A , CM000680.1:g.3879648G>A	GRCh37
NC_000018.8:g.3869648G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004746.4:c.421C>T (DLGAP1) MANE Select	NP_004737.2:p.Leu141=
ENST00000315677.8:c.421C>T (DLGAP1) MANE Select	ENSP00000316377.3:p.Leu141=
NM_001242761.1:c.421C>T (DLGAP1)	NP_001229690.1:p.Leu141=
NM_001242761.2:c.421C>T (DLGAP1)	NP_001229690.1:p.Leu141=
NM_001398525.1:c.421C>T (DLGAP1)	NP_001385454.1:p.Leu141=
NM_001398526.1:c.421C>T (DLGAP1)	NP_001385455.1:p.Leu141=
NM_001398527.1:c.421C>T (DLGAP1)	NP_001385456.1:p.Leu141=
NM_001398528.1:c.421C>T (DLGAP1)	NP_001385457.1:p.Leu141=
NM_004746.3:c.421C>T (DLGAP1)	NP_004737.2:p.Leu141=
NR_038895.1:n.112+1357G>A (DLGAP1-AS3)
ENST00000315677.7:c.421C>T (DLGAP1)	ENSP00000316377.3:p.Leu141=
ENST00000498188.5:n.429C>T (DLGAP1)
ENST00000581527.5:c.421C>T (DLGAP1)	ENSP00000463864.1:p.Leu141=
ENST00000584874.5:c.421C>T (DLGAP1)	ENSP00000462882.1:p.Leu141=
ENST00000639615.1:c.421C>T (DLGAP1)	ENSP00000491005.1:p.Leu141=
XM_005258171.1:c.421C>T (DLGAP1)	XP_005258228.1:p.Leu141=
XM_005258171.3:c.421C>T (DLGAP1)	XP_005258228.1:p.Leu141=
XM_005258172.1:c.421C>T (DLGAP1)	XP_005258229.1:p.Leu141=
XM_011525770.1:c.421C>T (DLGAP1)	XP_011524072.1:p.Leu141=
XM_011525770.3:c.421C>T (DLGAP1)	XP_011524072.1:p.Leu141=
XM_011525771.1:c.421C>T (DLGAP1)	XP_011524073.1:p.Leu141=
XM_011525771.3:c.421C>T (DLGAP1)	XP_011524073.1:p.Leu141=
XM_024451288.1:c.421C>T (DLGAP1)	XP_024307056.1:p.Leu141=
XR_935073.1:n.992C>T (DLGAP1)
XR_935107.1:n.460+1241G>A