Canonical Allele Identifier: CA8773437

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75842428C>T , CM000679.2:g.75842428C>T	GRCh38
NC_000017.10:g.73838509C>T , CM000679.1:g.73838509C>T	GRCh37
NC_000017.9:g.71350104C>T	NCBI36
NG_007266.1:g.7290G>A , LRG_122:g.7290G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.569+5G>A MANE Select	NP_954712.1:n.569+5G>A
ENST00000207549.9:c.569+5G>A MANE Select	ENSP00000207549.3:n.569+5G>A
NM_199242.2:c.569+5G>A , LRG_122t1:c.569+5G>A	NP_954712.1:n.569+5G>A
ENST00000207549.8:c.569+5G>A	ENSP00000207549.3:n.569+5G>A
ENST00000412096.6:c.569+5G>A	ENSP00000388093.1:n.569+5G>A
ENST00000585574.5:n.545+5G>A
ENST00000585574.6:c.512+5G>A	ENSP00000514389.1:n.512+5G>A
ENST00000586147.1:c.117+1793G>A	ENSP00000466543.1:n.117+1793G>A
ENST00000587504.5:n.534+5G>A
ENST00000587504.6:c.512+5G>A	ENSP00000514388.1:n.512+5G>A
ENST00000590762.5:c.512+5G>A	ENSP00000467653.1:n.512+5G>A
ENST00000591563.5:n.650+5G>A
ENST00000592386.5:c.548+5G>A	ENSP00000466826.1:n.548+5G>A
ENST00000592386.6:c.551+5G>A	ENSP00000466826.2:n.551+5G>A
ENST00000699512.1:c.409G>A
XM_011524504.1:c.569+5G>A	XP_011522806.1:n.569+5G>A
XM_011524504.2:c.569+5G>A	XP_011522806.1:n.569+5G>A
XM_011524505.1:c.569+5G>A	XP_011522807.1:n.569+5G>A
XM_011524506.1:c.569+5G>A	XP_011522808.1:n.569+5G>A
XM_011524507.1:c.-41+5G>A	XP_011522809.1:n.-41+5G>A
XM_011524507.2:c.-41+5G>A	XP_011522809.1:n.-41+5G>A