Canonical Allele Identifier: CA502050232

Gene: UNC13D

Linked Data

• MyVariant Identifiers: chr17:g.73832420C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75836339C>T , CM000679.2:g.75836339C>T	GRCh38
NC_000017.10:g.73832420C>T , CM000679.1:g.73832420C>T	GRCh37
NC_000017.9:g.71344015C>T	NCBI36
NG_007266.1:g.13379G>A , LRG_122:g.13379G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000699510.1:c.324G>A	ENSP00000514405.1:p.Gln108=
ENST00000699511.1:c.566G>A
ENST00000207549.9:c.1389G>A MANE Select	ENSP00000207549.3:p.Gln463=
ENST00000207549.8:c.1389G>A	ENSP00000207549.3:p.Gln463=
ENST00000412096.6:c.1389G>A	ENSP00000388093.1:p.Gln463=
ENST00000586147.1:c.118-83G>A	ENSP00000466543.1:n.118-83G>A
ENST00000587105.1:c.508G>A
ENST00000591563.5:n.1659G>A
NM_199242.2:c.1389G>A , LRG_122t1:c.1389G>A	NP_954712.1:p.Gln463=
XM_011524504.1:c.1389G>A	XP_011522806.1:p.Gln463=
XM_011524505.1:c.1389G>A	XP_011522807.1:p.Gln463=
XM_011524506.1:c.1386G>A	XP_011522808.1:p.Gln462=
XM_011524507.1:c.780G>A	XP_011522809.1:p.Gln260=
XM_011524508.1:c.780G>A	XP_011522810.1:p.Gln260=
XM_011524504.2:c.1389G>A	XP_011522806.1:p.Gln463=
XM_011524507.2:c.780G>A	XP_011522809.1:p.Gln260=
XM_024450640.1:c.780G>A	XP_024306408.1:p.Gln260=
NM_199242.3:c.1389G>A MANE Select	NP_954712.1:p.Gln463=