Canonical Allele Identifier: CA8773178

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75839922G>A , CM000679.2:g.75839922G>A	GRCh38
NC_000017.10:g.73836003G>A , CM000679.1:g.73836003G>A	GRCh37
NC_000017.9:g.71347598G>A	NCBI36
NG_007266.1:g.9796C>T , LRG_122:g.9796C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.972C>T MANE Select	NP_954712.1:p.Asp324=
ENST00000207549.9:c.972C>T MANE Select	ENSP00000207549.3:p.Asp324=
NM_199242.2:c.972C>T , LRG_122t1:c.972C>T	NP_954712.1:p.Asp324=
ENST00000207549.8:c.972C>T	ENSP00000207549.3:p.Asp324=
ENST00000412096.6:c.972C>T	ENSP00000388093.1:p.Asp324=
ENST00000586147.1:c.118-3666C>T	ENSP00000466543.1:n.118-3666C>T
ENST00000587105.1:c.194C>T
ENST00000587504.5:n.975C>T
ENST00000587504.6:c.953C>T	ENSP00000514388.1:p.Thr318Met
ENST00000591563.5:n.1242C>T
ENST00000699511.1:c.152C>T
XM_011524504.1:c.972C>T	XP_011522806.1:p.Asp324=
XM_011524504.2:c.972C>T	XP_011522806.1:p.Asp324=
XM_011524505.1:c.972C>T	XP_011522807.1:p.Asp324=
XM_011524506.1:c.972C>T	XP_011522808.1:p.Asp324=
XM_011524507.1:c.363C>T	XP_011522809.1:p.Asp121=
XM_011524507.2:c.363C>T	XP_011522809.1:p.Asp121=
XM_011524508.1:c.363C>T	XP_011522810.1:p.Asp121=
XM_024450640.1:c.363C>T	XP_024306408.1:p.Asp121=