Canonical Allele Identifier: CA2275708999
Gene: UNC13D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75840520A= , CM000679.2:g.75840520A= GRCh38
NC_000017.10:g.73836601A= , CM000679.1:g.73836601A= GRCh37
NC_000017.9:g.71348196A= NCBI36
NG_007266.1:g.9198T= , LRG_122:g.9198T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000585574.6:c.*162T= ENSP00000514389.1:n.*162T=
ENST00000587504.6:c.683T= ENSP00000514388.1:p.Val228=
ENST00000592386.6:c.722T= ENSP00000466826.2:p.Val241=
ENST00000207549.9:c.740T= MANE Select ENSP00000207549.3:p.Val247=
ENST00000207549.8:c.740T= ENSP00000207549.3:p.Val247=
ENST00000412096.6:c.740T= ENSP00000388093.1:p.Val247=
ENST00000586147.1:c.117+3701T= ENSP00000466543.1:n.117+3701T=
ENST00000587504.5:n.705T=
ENST00000590762.5:c.683T= ENSP00000467653.1:p.Val228=
ENST00000591563.5:n.821T=
ENST00000592386.5:c.719T= ENSP00000466826.1:p.Val240=
NM_199242.2:c.740T= , LRG_122t1:c.740T= NP_954712.1:p.Val247=
XM_011524504.1:c.740T= XP_011522806.1:p.Val247=
XM_011524505.1:c.740T= XP_011522807.1:p.Val247=
XM_011524506.1:c.740T= XP_011522808.1:p.Val247=
XM_011524507.1:c.131T= XP_011522809.1:p.Val44=
XM_011524508.1:c.131T= XP_011522810.1:p.Val44=
XM_011524504.2:c.740T= XP_011522806.1:p.Val247=
XM_011524507.2:c.131T= XP_011522809.1:p.Val44=
XM_024450640.1:c.131T= XP_024306408.1:p.Val44=
NM_199242.3:c.740T= MANE Select NP_954712.1:p.Val247=