Canonical Allele Identifier: CA2275706897

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75836239C= , CM000679.2:g.75836239C=	GRCh38
NC_000017.10:g.73832320C= , CM000679.1:g.73832320C=	GRCh37
NC_000017.9:g.71343915C=	NCBI36
NG_007266.1:g.13479G= , LRG_122:g.13479G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699510.1:c.342G=	ENSP00000514405.1:p.Trp114=
ENST00000699511.1:c.584G=
ENST00000207549.9:c.1407G= MANE Select	ENSP00000207549.3:p.Trp469=
ENST00000207549.8:c.1407G=	ENSP00000207549.3:p.Trp469=
ENST00000412096.6:c.1407G=	ENSP00000388093.1:p.Trp469=
ENST00000586147.1:c.135G=	ENSP00000466543.1:p.Trp45=
ENST00000587105.1:c.526G=
ENST00000591563.5:n.1677G=
NM_199242.2:c.1407G= , LRG_122t1:c.1407G=	NP_954712.1:p.Trp469=
XM_011524504.1:c.1407G=	XP_011522806.1:p.Trp469=
XM_011524505.1:c.1407G=	XP_011522807.1:p.Trp469=
XM_011524506.1:c.1404G=	XP_011522808.1:p.Trp468=
XM_011524507.1:c.798G=	XP_011522809.1:p.Trp266=
XM_011524508.1:c.798G=	XP_011522810.1:p.Trp266=
XM_011524504.2:c.1407G=	XP_011522806.1:p.Trp469=
XM_011524507.2:c.798G=	XP_011522809.1:p.Trp266=
XM_024450640.1:c.798G=	XP_024306408.1:p.Trp266=
NM_199242.3:c.1407G= MANE Select	NP_954712.1:p.Trp469=