Canonical Allele Identifier: CA2275704433

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75831153A= , CM000679.2:g.75831153A=	GRCh38
NC_000017.10:g.73827234A= , CM000679.1:g.73827234A=	GRCh37
NC_000017.9:g.71338829A=	NCBI36
NG_007266.1:g.18565T= , LRG_122:g.18565T=

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.2570T= MANE Select	NP_954712.1:p.Phe857=
ENST00000207549.9:c.2570T= MANE Select	ENSP00000207549.3:p.Phe857=
NM_199242.2:c.2570T= , LRG_122t1:c.2570T=	NP_954712.1:p.Phe857=
ENST00000207549.8:c.2570T=	ENSP00000207549.3:p.Phe857=
ENST00000412096.6:c.2570T=	ENSP00000388093.1:p.Phe857=
ENST00000699510.1:c.1436T=	ENSP00000514405.1:p.Phe479=
XM_011524504.1:c.2639T=	XP_011522806.1:p.Phe880=
XM_011524504.2:c.2639T=	XP_011522806.1:p.Phe880=
XM_011524505.1:c.2639T=	XP_011522807.1:p.Phe880=
XM_011524506.1:c.2636T=	XP_011522808.1:p.Phe879=
XM_011524507.1:c.2030T=	XP_011522809.1:p.Phe677=
XM_011524507.2:c.2030T=	XP_011522809.1:p.Phe677=
XM_011524508.1:c.2030T=	XP_011522810.1:p.Phe677=
XM_024450640.1:c.2030T=	XP_024306408.1:p.Phe677=