Canonical Allele Identifier: CA2275708774

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75840050G= , CM000679.2:g.75840050G=	GRCh38
NC_000017.10:g.73836131G= , CM000679.1:g.73836131G=	GRCh37
NC_000017.9:g.71347726G=	NCBI36
NG_007266.1:g.9668C= , LRG_122:g.9668C=

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.919C= MANE Select	NP_954712.1:p.Gln307=
ENST00000207549.9:c.919C= MANE Select	ENSP00000207549.3:p.Gln307=
NM_199242.2:c.919C= , LRG_122t1:c.919C=	NP_954712.1:p.Gln307=
ENST00000207549.8:c.919C=	ENSP00000207549.3:p.Gln307=
ENST00000412096.6:c.919C=	ENSP00000388093.1:p.Gln307=
ENST00000586147.1:c.118-3794C=	ENSP00000466543.1:n.118-3794C=
ENST00000587105.1:c.141C=
ENST00000587504.5:n.922C=
ENST00000587504.6:c.900C=	ENSP00000514388.1:p.Ser300=
ENST00000591563.5:n.1114C=
ENST00000592386.5:c.898C=	ENSP00000466826.1:p.Gln300=
ENST00000592386.6:c.901C=	ENSP00000466826.2:p.Gln301=
ENST00000699511.1:c.99C=
XM_011524504.1:c.919C=	XP_011522806.1:p.Gln307=
XM_011524504.2:c.919C=	XP_011522806.1:p.Gln307=
XM_011524505.1:c.919C=	XP_011522807.1:p.Gln307=
XM_011524506.1:c.919C=	XP_011522808.1:p.Gln307=
XM_011524507.1:c.310C=	XP_011522809.1:p.Gln104=
XM_011524507.2:c.310C=	XP_011522809.1:p.Gln104=
XM_011524508.1:c.310C=	XP_011522810.1:p.Gln104=
XM_024450640.1:c.310C=	XP_024306408.1:p.Gln104=