Canonical Allele Identifier: CA2275710742
Gene: UNC13D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75843828G= , CM000679.2:g.75843828G= GRCh38
NC_000017.10:g.73839909G= , CM000679.1:g.73839909G= GRCh37
NC_000017.9:g.71351504G= NCBI36
NG_007266.1:g.5890C= , LRG_122:g.5890C=

Transcript Alleles

HGVS Amino-acid change
ENST00000588774.2:n.596C=
ENST00000592386.6:c.118-309C= ENSP00000466826.2:n.118-309C=
ENST00000699512.1:c.13-309C= ENSP00000514407.1:n.13-309C=
ENST00000699513.1:c.118-309C= ENSP00000514408.1:n.118-309C=
ENST00000207549.9:c.118-309C= MANE Select ENSP00000207549.3:n.118-309C=
ENST00000207549.8:c.118-309C= ENSP00000207549.3:n.118-309C=
ENST00000412096.6:c.118-309C= ENSP00000388093.1:n.118-309C=
ENST00000586108.1:c.118-309C= ENSP00000464749.1:n.118-309C=
ENST00000586147.1:c.117+393C= ENSP00000466543.1:n.117+393C=
ENST00000588774.1:n.486C=
ENST00000591563.5:n.199-309C=
ENST00000592386.5:c.115-309C= ENSP00000466826.1:n.115-309C=
NM_199242.2:c.118-309C= , LRG_122t1:c.118-309C= NP_954712.1:n.118-309C=
XM_011524504.1:c.118-309C= XP_011522806.1:n.118-309C=
XM_011524505.1:c.118-309C= XP_011522807.1:n.118-309C=
XM_011524506.1:c.118-309C= XP_011522808.1:n.118-309C=
XM_011524507.1:c.-801C= XP_011522809.1:n.-801C=
XM_011524504.2:c.118-309C= XP_011522806.1:n.118-309C=
XM_011524507.2:c.-801C= XP_011522809.1:n.-801C=
NM_199242.3:c.118-309C= MANE Select NP_954712.1:n.118-309C=