Canonical Allele Identifier: CA502050438

Gene: UNC13D

Linked Data

• MyVariant Identifiers: chr17:g.73836123C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75840042C>A , CM000679.2:g.75840042C>A	GRCh38
NC_000017.10:g.73836123C>A , CM000679.1:g.73836123C>A	GRCh37
NC_000017.9:g.71347718C>A	NCBI36
NG_007266.1:g.9676G>T , LRG_122:g.9676G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587504.6:c.908G>T	ENSP00000514388.1:p.Cys303Phe
ENST00000592386.6:c.909G>T	ENSP00000466826.2:p.Val303=
ENST00000699511.1:c.107G>T
ENST00000207549.9:c.927G>T MANE Select	ENSP00000207549.3:p.Val309=
ENST00000207549.8:c.927G>T	ENSP00000207549.3:p.Val309=
ENST00000412096.6:c.927G>T	ENSP00000388093.1:p.Val309=
ENST00000586147.1:c.118-3786G>T	ENSP00000466543.1:n.118-3786G>T
ENST00000587105.1:c.149G>T
ENST00000587504.5:n.930G>T
ENST00000591563.5:n.1122G>T
ENST00000592386.5:c.906G>T	ENSP00000466826.1:p.Val302=
NM_199242.2:c.927G>T , LRG_122t1:c.927G>T	NP_954712.1:p.Val309=
XM_011524504.1:c.927G>T	XP_011522806.1:p.Val309=
XM_011524505.1:c.927G>T	XP_011522807.1:p.Val309=
XM_011524506.1:c.927G>T	XP_011522808.1:p.Val309=
XM_011524507.1:c.318G>T	XP_011522809.1:p.Val106=
XM_011524508.1:c.318G>T	XP_011522810.1:p.Val106=
XM_011524504.2:c.927G>T	XP_011522806.1:p.Val309=
XM_011524507.2:c.318G>T	XP_011522809.1:p.Val106=
XM_024450640.1:c.318G>T	XP_024306408.1:p.Val106=
NM_199242.3:c.927G>T MANE Select	NP_954712.1:p.Val309=