Canonical Allele Identifier: CA2275708898

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75840317G= , CM000679.2:g.75840317G=	GRCh38
NC_000017.10:g.73836398G= , CM000679.1:g.73836398G=	GRCh37
NC_000017.9:g.71347993G=	NCBI36
NG_007266.1:g.9401C= , LRG_122:g.9401C=

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.766C= MANE Select	NP_954712.1:p.Arg256=
ENST00000207549.9:c.766C= MANE Select	ENSP00000207549.3:p.Arg256=
NM_199242.2:c.766C= , LRG_122t1:c.766C=	NP_954712.1:p.Arg256=
ENST00000207549.8:c.766C=	ENSP00000207549.3:p.Arg256=
ENST00000412096.6:c.766C=	ENSP00000388093.1:p.Arg256=
ENST00000586147.1:c.117+3904C=	ENSP00000466543.1:n.117+3904C=
ENST00000587504.5:n.769C=
ENST00000587504.6:c.747C=	ENSP00000514388.1:p.Ala249=
ENST00000590762.5:c.709C=	ENSP00000467653.1:p.Arg237=
ENST00000591563.5:n.847C=
ENST00000592386.5:c.745C=	ENSP00000466826.1:p.Arg249=
ENST00000592386.6:c.748C=	ENSP00000466826.2:p.Arg250=
XM_011524504.1:c.766C=	XP_011522806.1:p.Arg256=
XM_011524504.2:c.766C=	XP_011522806.1:p.Arg256=
XM_011524505.1:c.766C=	XP_011522807.1:p.Arg256=
XM_011524506.1:c.766C=	XP_011522808.1:p.Arg256=
XM_011524507.1:c.157C=	XP_011522809.1:p.Arg53=
XM_011524507.2:c.157C=	XP_011522809.1:p.Arg53=
XM_011524508.1:c.157C=	XP_011522810.1:p.Arg53=
XM_024450640.1:c.157C=	XP_024306408.1:p.Arg53=