Canonical Allele Identifier: CA294084276

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75828984C>T , CM000679.2:g.75828984C>T	GRCh38
NC_000017.10:g.73825065C>T , CM000679.1:g.73825065C>T	GRCh37
NC_000017.9:g.71336660C>T	NCBI36
NG_007266.1:g.20734G>A , LRG_122:g.20734G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.2955-1G>A MANE Select	NP_954712.1:n.2955-1G>A
ENST00000207549.9:c.2955-1G>A MANE Select	ENSP00000207549.3:n.2955-1G>A
NM_199242.2:c.2955-1G>A , LRG_122t1:c.2955-1G>A	NP_954712.1:n.2955-1G>A
ENST00000207549.8:c.2955-1G>A	ENSP00000207549.3:n.2955-1G>A
ENST00000412096.6:c.2955-1G>A	ENSP00000388093.1:n.2955-1G>A
ENST00000586519.1:c.77-1G>A	ENSP00000466149.1:n.77-1G>A
ENST00000589670.5:c.121-1G>A
ENST00000699510.1:c.1821-1G>A	ENSP00000514405.1:n.1821-1G>A
XM_011524504.1:c.3024-1G>A	XP_011522806.1:n.3024-1G>A
XM_011524504.2:c.3024-1G>A	XP_011522806.1:n.3024-1G>A
XM_011524505.1:c.3024-1G>A	XP_011522807.1:n.3024-1G>A
XM_011524506.1:c.3021-1G>A	XP_011522808.1:n.3021-1G>A
XM_011524507.1:c.2415-1G>A	XP_011522809.1:n.2415-1G>A
XM_011524507.2:c.2415-1G>A	XP_011522809.1:n.2415-1G>A
XM_011524508.1:c.2415-1G>A	XP_011522810.1:n.2415-1G>A
XM_024450640.1:c.2415-1G>A	XP_024306408.1:n.2415-1G>A