Canonical Allele Identifier: CA401078617

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75830131G>A , CM000679.2:g.75830131G>A	GRCh38
NC_000017.10:g.73826212G>A , CM000679.1:g.73826212G>A	GRCh37
NC_000017.9:g.71337807G>A	NCBI36
NG_007266.1:g.19587C>T , LRG_122:g.19587C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.2851C>T MANE Select	NP_954712.1:p.Gln951Ter
ENST00000207549.9:c.2851C>T MANE Select	ENSP00000207549.3:p.Gln951Ter
NM_199242.2:c.2851C>T , LRG_122t1:c.2851C>T	NP_954712.1:p.Gln951Ter
ENST00000207549.8:c.2851C>T	ENSP00000207549.3:p.Gln951Ter
ENST00000412096.6:c.2851C>T	ENSP00000388093.1:p.Gln951Ter
ENST00000586519.1:c.76+231C>T	ENSP00000466149.1:n.76+231C>T
ENST00000589670.5:c.17C>T
ENST00000590856.1:n.226C>T
ENST00000699510.1:c.1717C>T	ENSP00000514405.1:p.Gln573Ter
XM_011524504.1:c.2920C>T	XP_011522806.1:p.Gln974Ter
XM_011524504.2:c.2920C>T	XP_011522806.1:p.Gln974Ter
XM_011524505.1:c.2920C>T	XP_011522807.1:p.Gln974Ter
XM_011524506.1:c.2917C>T	XP_011522808.1:p.Gln973Ter
XM_011524507.1:c.2311C>T	XP_011522809.1:p.Gln771Ter
XM_011524507.2:c.2311C>T	XP_011522809.1:p.Gln771Ter
XM_011524508.1:c.2311C>T	XP_011522810.1:p.Gln771Ter
XM_024450640.1:c.2311C>T	XP_024306408.1:p.Gln771Ter