Canonical Allele Identifier: CA401075003

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75828920G>C , CM000679.2:g.75828920G>C	GRCh38
NC_000017.10:g.73825001G>C , CM000679.1:g.73825001G>C	GRCh37
NC_000017.9:g.71336596G>C	NCBI36
NG_007266.1:g.20798C>G , LRG_122:g.20798C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.3018C>G MANE Select	NP_954712.1:p.Tyr1006Ter
ENST00000207549.9:c.3018C>G MANE Select	ENSP00000207549.3:p.Tyr1006Ter
NM_199242.2:c.3018C>G , LRG_122t1:c.3018C>G	NP_954712.1:p.Tyr1006Ter
ENST00000207549.8:c.3018C>G	ENSP00000207549.3:p.Tyr1006Ter
ENST00000412096.6:c.3018C>G	ENSP00000388093.1:p.Tyr1006Ter
ENST00000586519.1:c.140C>G	ENSP00000466149.1:p.Thr47Arg
ENST00000589670.5:c.184C>G
ENST00000699510.1:c.1884C>G	ENSP00000514405.1:p.Tyr628Ter
XM_011524504.1:c.3087C>G	XP_011522806.1:p.Tyr1029Ter
XM_011524504.2:c.3087C>G	XP_011522806.1:p.Tyr1029Ter
XM_011524505.1:c.3087C>G	XP_011522807.1:p.Tyr1029Ter
XM_011524506.1:c.3084C>G	XP_011522808.1:p.Tyr1028Ter
XM_011524507.1:c.2478C>G	XP_011522809.1:p.Tyr826Ter
XM_011524507.2:c.2478C>G	XP_011522809.1:p.Tyr826Ter
XM_011524508.1:c.2478C>G	XP_011522810.1:p.Tyr826Ter
XM_024450640.1:c.2478C>G	XP_024306408.1:p.Tyr826Ter