Canonical Allele Identifier: CA501844986

Gene: UNC13D

Linked Data

• MyVariant Identifiers: chr17:g.73836596T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75840515T>G , CM000679.2:g.75840515T>G	GRCh38
NC_000017.10:g.73836596T>G , CM000679.1:g.73836596T>G	GRCh37
NC_000017.9:g.71348191T>G	NCBI36
NG_007266.1:g.9203A>C , LRG_122:g.9203A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585574.6:c.*167A>C	ENSP00000514389.1:n.*167A>C
ENST00000587504.6:c.688A>C	ENSP00000514388.1:p.Arg230=
ENST00000592386.6:c.727A>C	ENSP00000466826.2:p.Arg243=
ENST00000207549.9:c.745A>C MANE Select	ENSP00000207549.3:p.Arg249=
ENST00000207549.8:c.745A>C	ENSP00000207549.3:p.Arg249=
ENST00000412096.6:c.745A>C	ENSP00000388093.1:p.Arg249=
ENST00000586147.1:c.117+3706A>C	ENSP00000466543.1:n.117+3706A>C
ENST00000587504.5:n.710A>C
ENST00000590762.5:c.688A>C	ENSP00000467653.1:p.Arg230=
ENST00000591563.5:n.826A>C
ENST00000592386.5:c.724A>C	ENSP00000466826.1:p.Arg242=
NM_199242.2:c.745A>C , LRG_122t1:c.745A>C	NP_954712.1:p.Arg249=
XM_011524504.1:c.745A>C	XP_011522806.1:p.Arg249=
XM_011524505.1:c.745A>C	XP_011522807.1:p.Arg249=
XM_011524506.1:c.745A>C	XP_011522808.1:p.Arg249=
XM_011524507.1:c.136A>C	XP_011522809.1:p.Arg46=
XM_011524508.1:c.136A>C	XP_011522810.1:p.Arg46=
XM_011524504.2:c.745A>C	XP_011522806.1:p.Arg249=
XM_011524507.2:c.136A>C	XP_011522809.1:p.Arg46=
XM_024450640.1:c.136A>C	XP_024306408.1:p.Arg46=
NM_199242.3:c.745A>C MANE Select	NP_954712.1:p.Arg249=