Canonical Allele Identifier: CA2275706948

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75836345G= , CM000679.2:g.75836345G=	GRCh38
NC_000017.10:g.73832426G= , CM000679.1:g.73832426G=	GRCh37
NC_000017.9:g.71344021G=	NCBI36
NG_007266.1:g.13373C= , LRG_122:g.13373C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699510.1:c.318C=	ENSP00000514405.1:p.Ala106=
ENST00000699511.1:c.560C=
ENST00000207549.9:c.1383C= MANE Select	ENSP00000207549.3:p.Ala461=
ENST00000207549.8:c.1383C=	ENSP00000207549.3:p.Ala461=
ENST00000412096.6:c.1383C=	ENSP00000388093.1:p.Ala461=
ENST00000586147.1:c.118-89C=	ENSP00000466543.1:n.118-89C=
ENST00000587105.1:c.502C=
ENST00000591563.5:n.1653C=
NM_199242.2:c.1383C= , LRG_122t1:c.1383C=	NP_954712.1:p.Ala461=
XM_011524504.1:c.1383C=	XP_011522806.1:p.Ala461=
XM_011524505.1:c.1383C=	XP_011522807.1:p.Ala461=
XM_011524506.1:c.1380C=	XP_011522808.1:p.Ala460=
XM_011524507.1:c.774C=	XP_011522809.1:p.Ala258=
XM_011524508.1:c.774C=	XP_011522810.1:p.Ala258=
XM_011524504.2:c.1383C=	XP_011522806.1:p.Ala461=
XM_011524507.2:c.774C=	XP_011522809.1:p.Ala258=
XM_024450640.1:c.774C=	XP_024306408.1:p.Ala258=
NM_199242.3:c.1383C= MANE Select	NP_954712.1:p.Ala461=