Canonical Allele Identifier: CA2275706566

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75835570_75835571delinsAC , CM000679.2:g.75835570_75835571delinsAC	GRCh38
NC_000017.10:g.73831651_73831652delinsAC , CM000679.1:g.73831651_73831652delinsAC	GRCh37
NC_000017.9:g.71343246_71343247delinsAC	NCBI36
NG_007266.1:g.14147_14148delinsGT , LRG_122:g.14147_14148delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000699510.1:c.663-42_663-41delinsGT	ENSP00000514405.1:n.663-42_663-41delinsGT...
ENST00000207549.9:c.1728-42_1728-41delinsGT MANE Select	ENSP00000207549.3:n.1728-42_1728-41delins...
ENST00000207549.8:c.1728-42_1728-41delinsGT	ENSP00000207549.3:n.1728-42_1728-41delins...
ENST00000412096.6:c.1728-42_1728-41delinsGT	ENSP00000388093.1:n.1728-42_1728-41delins...
ENST00000586147.1:c.456-42_456-41delinsGT	ENSP00000466543.1:n.456-42_456-41delinsGT...
ENST00000591563.5:n.1998-42_1998-41delinsGT
NM_199242.2:c.1728-42_1728-41delinsGT , LRG_122t1:c.1728-42_1728-41delinsGT	NP_954712.1:n.1728-42_1728-41delinsGT
XM_011524504.1:c.1728-42_1728-41delinsGT	XP_011522806.1:n.1728-42_1728-41delinsGT
XM_011524505.1:c.1728-42_1728-41delinsGT	XP_011522807.1:n.1728-42_1728-41delinsGT
XM_011524506.1:c.1725-42_1725-41delinsGT	XP_011522808.1:n.1725-42_1725-41delinsGT
XM_011524507.1:c.1119-42_1119-41delinsGT	XP_011522809.1:n.1119-42_1119-41delinsGT
XM_011524508.1:c.1119-42_1119-41delinsGT	XP_011522810.1:n.1119-42_1119-41delinsGT
XM_011524504.2:c.1728-42_1728-41delinsGT	XP_011522806.1:n.1728-42_1728-41delinsGT
XM_011524507.2:c.1119-42_1119-41delinsGT	XP_011522809.1:n.1119-42_1119-41delinsGT
XM_024450640.1:c.1119-42_1119-41delinsGT	XP_024306408.1:n.1119-42_1119-41delinsGT
NM_199242.3:c.1728-42_1728-41delinsGT MANE Select	NP_954712.1:n.1728-42_1728-41delinsGT