Canonical Allele Identifier: CA2639898130

Gene: UNC13D

Linked Data

• gnomAD v4: 17-75843732-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75843732G>T , CM000679.2:g.75843732G>T	GRCh38
NC_000017.10:g.73839813G>T , CM000679.1:g.73839813G>T	GRCh37
NC_000017.9:g.71351408G>T	NCBI36
NG_007266.1:g.5986C>A , LRG_122:g.5986C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000585574.6:c.-10C>A	ENSP00000514389.1:n.-10C>A
ENST00000587504.6:c.-10C>A	ENSP00000514388.1:n.-10C>A
ENST00000588774.2:n.692C>A
ENST00000592386.6:c.118-213C>A	ENSP00000466826.2:n.118-213C>A
ENST00000699512.1:c.13-213C>A	ENSP00000514407.1:n.13-213C>A
ENST00000699513.1:c.118-213C>A	ENSP00000514408.1:n.118-213C>A
ENST00000207549.9:c.118-213C>A MANE Select	ENSP00000207549.3:n.118-213C>A
ENST00000207549.8:c.118-213C>A	ENSP00000207549.3:n.118-213C>A
ENST00000412096.6:c.118-213C>A	ENSP00000388093.1:n.118-213C>A
ENST00000585574.5:n.24C>A
ENST00000586108.1:c.118-213C>A	ENSP00000464749.1:n.118-213C>A
ENST00000586147.1:c.117+489C>A	ENSP00000466543.1:n.117+489C>A
ENST00000587504.5:n.13C>A
ENST00000588774.1:n.582C>A
ENST00000590762.5:c.-10C>A	ENSP00000467653.1:n.-10C>A
ENST00000591563.5:n.199-213C>A
ENST00000592386.5:c.115-213C>A	ENSP00000466826.1:n.115-213C>A
NM_199242.2:c.118-213C>A , LRG_122t1:c.118-213C>A	NP_954712.1:n.118-213C>A
XM_011524504.1:c.118-213C>A	XP_011522806.1:n.118-213C>A
XM_011524505.1:c.118-213C>A	XP_011522807.1:n.118-213C>A
XM_011524506.1:c.118-213C>A	XP_011522808.1:n.118-213C>A
XM_011524507.1:c.-705C>A	XP_011522809.1:n.-705C>A
XM_011524504.2:c.118-213C>A	XP_011522806.1:n.118-213C>A
XM_011524507.2:c.-705C>A	XP_011522809.1:n.-705C>A
NM_199242.3:c.118-213C>A MANE Select	NP_954712.1:n.118-213C>A