Canonical Allele Identifier: CA2275710744
Gene: UNC13D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75843832T= , CM000679.2:g.75843832T= GRCh38
NC_000017.10:g.73839913T= , CM000679.1:g.73839913T= GRCh37
NC_000017.9:g.71351508T= NCBI36
NG_007266.1:g.5886A= , LRG_122:g.5886A=

Transcript Alleles

HGVS Amino-acid change
ENST00000588774.2:n.592A=
ENST00000592386.6:c.118-313A= ENSP00000466826.2:n.118-313A=
ENST00000699512.1:c.13-313A= ENSP00000514407.1:n.13-313A=
ENST00000699513.1:c.118-313A= ENSP00000514408.1:n.118-313A=
ENST00000207549.9:c.118-313A= MANE Select ENSP00000207549.3:n.118-313A=
ENST00000207549.8:c.118-313A= ENSP00000207549.3:n.118-313A=
ENST00000412096.6:c.118-313A= ENSP00000388093.1:n.118-313A=
ENST00000586108.1:c.118-313A= ENSP00000464749.1:n.118-313A=
ENST00000586147.1:c.117+389A= ENSP00000466543.1:n.117+389A=
ENST00000588774.1:n.482A=
ENST00000591563.5:n.199-313A=
ENST00000592386.5:c.115-313A= ENSP00000466826.1:n.115-313A=
NM_199242.2:c.118-313A= , LRG_122t1:c.118-313A= NP_954712.1:n.118-313A=
XM_011524504.1:c.118-313A= XP_011522806.1:n.118-313A=
XM_011524505.1:c.118-313A= XP_011522807.1:n.118-313A=
XM_011524506.1:c.118-313A= XP_011522808.1:n.118-313A=
XM_011524507.1:c.-805A= XP_011522809.1:n.-805A=
XM_011524504.2:c.118-313A= XP_011522806.1:n.118-313A=
XM_011524507.2:c.-805A= XP_011522809.1:n.-805A=
NM_199242.3:c.118-313A= MANE Select NP_954712.1:n.118-313A=