Canonical Allele Identifier: CA8773011

Gene: UNC13D

Linked Data

• ClinVar Variation Id: 2995068
• ClinVar RCV Id: RCV003850675
• dbSNP Id: rs764237993
• ExAC: 17:73832426 G / A
• gnomAD v2: 17-73832426-G-A
• gnomAD v3: 17-75836345-G-A
• gnomAD v4: 17-75836345-G-A
• MyVariant Identifiers: chr17:g.73832426G>A (hg19) ; chr17:g.75836345G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75836345G>A , CM000679.2:g.75836345G>A	GRCh38
NC_000017.10:g.73832426G>A , CM000679.1:g.73832426G>A	GRCh37
NC_000017.9:g.71344021G>A	NCBI36
NG_007266.1:g.13373C>T , LRG_122:g.13373C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000699510.1:c.318C>T	ENSP00000514405.1:p.Ala106=
ENST00000699511.1:c.560C>T
ENST00000207549.9:c.1383C>T MANE Select	ENSP00000207549.3:p.Ala461=
ENST00000207549.8:c.1383C>T	ENSP00000207549.3:p.Ala461=
ENST00000412096.6:c.1383C>T	ENSP00000388093.1:p.Ala461=
ENST00000586147.1:c.118-89C>T	ENSP00000466543.1:n.118-89C>T
ENST00000587105.1:c.502C>T
ENST00000591563.5:n.1653C>T
NM_199242.2:c.1383C>T , LRG_122t1:c.1383C>T	NP_954712.1:p.Ala461=
XM_011524504.1:c.1383C>T	XP_011522806.1:p.Ala461=
XM_011524505.1:c.1383C>T	XP_011522807.1:p.Ala461=
XM_011524506.1:c.1380C>T	XP_011522808.1:p.Ala460=
XM_011524507.1:c.774C>T	XP_011522809.1:p.Ala258=
XM_011524508.1:c.774C>T	XP_011522810.1:p.Ala258=
XM_011524504.2:c.1383C>T	XP_011522806.1:p.Ala461=
XM_011524507.2:c.774C>T	XP_011522809.1:p.Ala258=
XM_024450640.1:c.774C>T	XP_024306408.1:p.Ala258=
NM_199242.3:c.1383C>T MANE Select	NP_954712.1:p.Ala461=