Canonical Allele Identifier: CA2275706436

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75835410T= , CM000679.2:g.75835410T=	GRCh38
NC_000017.10:g.73831491T= , CM000679.1:g.73831491T=	GRCh37
NC_000017.9:g.71343086T=	NCBI36
NG_007266.1:g.14308A= , LRG_122:g.14308A=

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.1847A= MANE Select	NP_954712.1:p.Glu616=
ENST00000207549.9:c.1847A= MANE Select	ENSP00000207549.3:p.Glu616=
NM_199242.2:c.1847A= , LRG_122t1:c.1847A=	NP_954712.1:p.Glu616=
ENST00000207549.8:c.1847A=	ENSP00000207549.3:p.Glu616=
ENST00000412096.6:c.1847A=	ENSP00000388093.1:p.Glu616=
ENST00000591563.5:n.2117A=
ENST00000699510.1:c.782A=	ENSP00000514405.1:p.Glu261=
XM_011524504.1:c.1847A=	XP_011522806.1:p.Glu616=
XM_011524504.2:c.1847A=	XP_011522806.1:p.Glu616=
XM_011524505.1:c.1847A=	XP_011522807.1:p.Glu616=
XM_011524506.1:c.1844A=	XP_011522808.1:p.Glu615=
XM_011524507.1:c.1238A=	XP_011522809.1:p.Glu413=
XM_011524507.2:c.1238A=	XP_011522809.1:p.Glu413=
XM_011524508.1:c.1238A=	XP_011522810.1:p.Glu413=
XM_024450640.1:c.1238A=	XP_024306408.1:p.Glu413=