Canonical Allele Identifier: CA1139665881

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75840750T>G , CM000679.2:g.75840750T>G	GRCh38
NC_000017.10:g.73836831T>G , CM000679.1:g.73836831T>G	GRCh37
NC_000017.9:g.71348426T>G	NCBI36
NG_007266.1:g.8968A>C , LRG_122:g.8968A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.683+12A>C MANE Select	NP_954712.1:n.683+12A>C
ENST00000207549.9:c.683+12A>C MANE Select	ENSP00000207549.3:n.683+12A>C
NM_199242.2:c.683+12A>C , LRG_122t1:c.683+12A>C	NP_954712.1:n.683+12A>C
ENST00000207549.8:c.683+12A>C	ENSP00000207549.3:n.683+12A>C
ENST00000412096.6:c.683+12A>C	ENSP00000388093.1:n.683+12A>C
ENST00000585574.6:c.*105+12A>C	ENSP00000514389.1:n.*105+12A>C
ENST00000586147.1:c.117+3471A>C	ENSP00000466543.1:n.117+3471A>C
ENST00000587504.5:n.648+12A>C
ENST00000587504.6:c.626+12A>C	ENSP00000514388.1:n.626+12A>C
ENST00000590762.5:c.626+12A>C	ENSP00000467653.1:n.626+12A>C
ENST00000591563.5:n.764+12A>C
ENST00000592386.5:c.662+12A>C	ENSP00000466826.1:n.662+12A>C
ENST00000592386.6:c.665+12A>C	ENSP00000466826.2:n.665+12A>C
XM_011524504.1:c.683+12A>C	XP_011522806.1:n.683+12A>C
XM_011524504.2:c.683+12A>C	XP_011522806.1:n.683+12A>C
XM_011524505.1:c.683+12A>C	XP_011522807.1:n.683+12A>C
XM_011524506.1:c.683+12A>C	XP_011522808.1:n.683+12A>C
XM_011524507.1:c.74+12A>C	XP_011522809.1:n.74+12A>C
XM_011524507.2:c.74+12A>C	XP_011522809.1:n.74+12A>C
XM_011524508.1:c.74+12A>C	XP_011522810.1:n.74+12A>C
XM_024450640.1:c.74+12A>C	XP_024306408.1:n.74+12A>C