Canonical Allele Identifier: CA8773435

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75842423G>A , CM000679.2:g.75842423G>A	GRCh38
NC_000017.10:g.73838504G>A , CM000679.1:g.73838504G>A	GRCh37
NC_000017.9:g.71350099G>A	NCBI36
NG_007266.1:g.7295C>T , LRG_122:g.7295C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.569+10C>T MANE Select	NP_954712.1:n.569+10C>T
ENST00000207549.9:c.569+10C>T MANE Select	ENSP00000207549.3:n.569+10C>T
NM_199242.2:c.569+10C>T , LRG_122t1:c.569+10C>T	NP_954712.1:n.569+10C>T
ENST00000207549.8:c.569+10C>T	ENSP00000207549.3:n.569+10C>T
ENST00000412096.6:c.569+10C>T	ENSP00000388093.1:n.569+10C>T
ENST00000585574.5:n.545+10C>T
ENST00000585574.6:c.512+10C>T	ENSP00000514389.1:n.512+10C>T
ENST00000586147.1:c.117+1798C>T	ENSP00000466543.1:n.117+1798C>T
ENST00000587504.5:n.534+10C>T
ENST00000587504.6:c.512+10C>T	ENSP00000514388.1:n.512+10C>T
ENST00000590762.5:c.512+10C>T	ENSP00000467653.1:n.512+10C>T
ENST00000591563.5:n.650+10C>T
ENST00000592386.5:c.548+10C>T	ENSP00000466826.1:n.548+10C>T
ENST00000592386.6:c.551+10C>T	ENSP00000466826.2:n.551+10C>T
XM_011524504.1:c.569+10C>T	XP_011522806.1:n.569+10C>T
XM_011524504.2:c.569+10C>T	XP_011522806.1:n.569+10C>T
XM_011524505.1:c.569+10C>T	XP_011522807.1:n.569+10C>T
XM_011524506.1:c.569+10C>T	XP_011522808.1:n.569+10C>T
XM_011524507.1:c.-41+10C>T	XP_011522809.1:n.-41+10C>T
XM_011524507.2:c.-41+10C>T	XP_011522809.1:n.-41+10C>T