Canonical Allele Identifier: CA2275708770

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75840040G= , CM000679.2:g.75840040G=	GRCh38
NC_000017.10:g.73836121G= , CM000679.1:g.73836121G=	GRCh37
NC_000017.9:g.71347716G=	NCBI36
NG_007266.1:g.9678C= , LRG_122:g.9678C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587504.6:c.910C=	ENSP00000514388.1:p.Pro304=
ENST00000592386.6:c.911C=	ENSP00000466826.2:p.Ser304=
ENST00000699511.1:c.109C=
ENST00000207549.9:c.929C= MANE Select	ENSP00000207549.3:p.Ser310=
ENST00000207549.8:c.929C=	ENSP00000207549.3:p.Ser310=
ENST00000412096.6:c.929C=	ENSP00000388093.1:p.Ser310=
ENST00000586147.1:c.118-3784C=	ENSP00000466543.1:n.118-3784C=
ENST00000587105.1:c.151C=
ENST00000587504.5:n.932C=
ENST00000591563.5:n.1124C=
ENST00000592386.5:c.908C=	ENSP00000466826.1:p.Ser303=
NM_199242.2:c.929C= , LRG_122t1:c.929C=	NP_954712.1:p.Ser310=
XM_011524504.1:c.929C=	XP_011522806.1:p.Ser310=
XM_011524505.1:c.929C=	XP_011522807.1:p.Ser310=
XM_011524506.1:c.929C=	XP_011522808.1:p.Ser310=
XM_011524507.1:c.320C=	XP_011522809.1:p.Ser107=
XM_011524508.1:c.320C=	XP_011522810.1:p.Ser107=
XM_011524504.2:c.929C=	XP_011522806.1:p.Ser310=
XM_011524507.2:c.320C=	XP_011522809.1:p.Ser107=
XM_024450640.1:c.320C=	XP_024306408.1:p.Ser107=
NM_199242.3:c.929C= MANE Select	NP_954712.1:p.Ser310=