Canonical Allele Identifier: CA2275708797

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75840100G= , CM000679.2:g.75840100G=	GRCh38
NC_000017.10:g.73836181G= , CM000679.1:g.73836181G=	GRCh37
NC_000017.9:g.71347776G=	NCBI36
NG_007266.1:g.9618C= , LRG_122:g.9618C=

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.869C= MANE Select	NP_954712.1:p.Ser290=
ENST00000207549.9:c.869C= MANE Select	ENSP00000207549.3:p.Ser290=
NM_199242.2:c.869C= , LRG_122t1:c.869C=	NP_954712.1:p.Ser290=
ENST00000207549.8:c.869C=	ENSP00000207549.3:p.Ser290=
ENST00000412096.6:c.869C=	ENSP00000388093.1:p.Ser290=
ENST00000586147.1:c.118-3844C=	ENSP00000466543.1:n.118-3844C=
ENST00000587105.1:c.91C=
ENST00000587504.5:n.872C=
ENST00000587504.6:c.850C=	ENSP00000514388.1:p.Arg284=
ENST00000591563.5:n.1064C=
ENST00000592386.5:c.848C=	ENSP00000466826.1:p.Ser283=
ENST00000592386.6:c.851C=	ENSP00000466826.2:p.Ser284=
ENST00000699511.1:c.49C=
XM_011524504.1:c.869C=	XP_011522806.1:p.Ser290=
XM_011524504.2:c.869C=	XP_011522806.1:p.Ser290=
XM_011524505.1:c.869C=	XP_011522807.1:p.Ser290=
XM_011524506.1:c.869C=	XP_011522808.1:p.Ser290=
XM_011524507.1:c.260C=	XP_011522809.1:p.Ser87=
XM_011524507.2:c.260C=	XP_011522809.1:p.Ser87=
XM_011524508.1:c.260C=	XP_011522810.1:p.Ser87=
XM_024450640.1:c.260C=	XP_024306408.1:p.Ser87=