Canonical Allele Identifier: CA14612730

Gene: DLGAP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.4133739T>C , CM000680.2:g.4133739T>C	GRCh38
NC_000018.9:g.4133739T>C , CM000680.1:g.4133739T>C	GRCh37
NC_000018.8:g.4123739T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315677.8:c.-159+17441A>G MANE Select	ENSP00000316377.3:n.-159+17441A>G
ENST00000639615.1:c.-159+17441A>G	ENSP00000491005.1:n.-159+17441A>G
ENST00000315677.7:c.-159+17441A>G	ENSP00000316377.3:n.-159+17441A>G
ENST00000577430.1:n.259+17441A>G
ENST00000578250.6:n.108+17441A>G
ENST00000581527.5:c.-159+17441A>G	ENSP00000463864.1:n.-159+17441A>G
ENST00000581550.5:n.237+17441A>G
ENST00000584874.5:c.-159+17441A>G	ENSP00000462882.1:n.-159+17441A>G
NM_001242761.1:c.-159+17441A>G	NP_001229690.1:n.-159+17441A>G
NM_004746.3:c.-159+17441A>G	NP_004737.2:n.-159+17441A>G
XM_005258171.1:c.-159+17441A>G	XP_005258228.1:n.-159+17441A>G
XM_005258172.1:c.-159+17441A>G	XP_005258229.1:n.-159+17441A>G
XM_011525770.1:c.-159+17441A>G	XP_011524072.1:n.-159+17441A>G
XM_011525771.1:c.-159+17441A>G	XP_011524073.1:n.-159+17441A>G
XR_935073.1:n.413+17441A>G
XM_005258171.3:c.-159+17441A>G	XP_005258228.1:n.-159+17441A>G
XM_011525770.3:c.-159+17441A>G	XP_011524072.1:n.-159+17441A>G
XM_011525771.3:c.-159+17441A>G	XP_011524073.1:n.-159+17441A>G
XM_024451288.1:c.-625+17441A>G	XP_024307056.1:n.-625+17441A>G
NM_004746.4:c.-159+17441A>G MANE Select	NP_004737.2:n.-159+17441A>G
NM_001242761.2:c.-159+17441A>G	NP_001229690.1:n.-159+17441A>G
NM_001398525.1:c.-159+17441A>G	NP_001385454.1:n.-159+17441A>G
NM_001398526.1:c.-159+17441A>G	NP_001385455.1:n.-159+17441A>G
NM_001398527.1:c.-159+17441A>G	NP_001385456.1:n.-159+17441A>G
NM_001398528.1:c.-159+17441A>G	NP_001385457.1:n.-159+17441A>G