Canonical Allele Identifier: CA2275706898

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75836246G= , CM000679.2:g.75836246G=	GRCh38
NC_000017.10:g.73832327G= , CM000679.1:g.73832327G=	GRCh37
NC_000017.9:g.71343922G=	NCBI36
NG_007266.1:g.13472C= , LRG_122:g.13472C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699510.1:c.335C=	ENSP00000514405.1:p.Thr112=
ENST00000699511.1:c.577C=
ENST00000207549.9:c.1400C= MANE Select	ENSP00000207549.3:p.Thr467=
ENST00000207549.8:c.1400C=	ENSP00000207549.3:p.Thr467=
ENST00000412096.6:c.1400C=	ENSP00000388093.1:p.Thr467=
ENST00000586147.1:c.128C=	ENSP00000466543.1:p.Thr43=
ENST00000587105.1:c.519C=
ENST00000591563.5:n.1670C=
NM_199242.2:c.1400C= , LRG_122t1:c.1400C=	NP_954712.1:p.Thr467=
XM_011524504.1:c.1400C=	XP_011522806.1:p.Thr467=
XM_011524505.1:c.1400C=	XP_011522807.1:p.Thr467=
XM_011524506.1:c.1397C=	XP_011522808.1:p.Thr466=
XM_011524507.1:c.791C=	XP_011522809.1:p.Thr264=
XM_011524508.1:c.791C=	XP_011522810.1:p.Thr264=
XM_011524504.2:c.1400C=	XP_011522806.1:p.Thr467=
XM_011524507.2:c.791C=	XP_011522809.1:p.Thr264=
XM_024450640.1:c.791C=	XP_024306408.1:p.Thr264=
NM_199242.3:c.1400C= MANE Select	NP_954712.1:p.Thr467=