Canonical Allele Identifier: CA627596559

Gene: UNC13D

Linked Data

• dbSNP Id: rs1233460229
• gnomAD v2: 17-73836082-C-T
• gnomAD v4: 17-75840001-C-T
• MyVariant Identifiers: chr17:g.73836082C>T (hg19) ; chr17:g.75840001C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75840001C>T , CM000679.2:g.75840001C>T	GRCh38
NC_000017.10:g.73836082C>T , CM000679.1:g.73836082C>T	GRCh37
NC_000017.9:g.71347677C>T	NCBI36
NG_007266.1:g.9717G>A , LRG_122:g.9717G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587504.6:c.932+17G>A	ENSP00000514388.1:n.932+17G>A
ENST00000699511.1:c.131+17G>A
ENST00000207549.9:c.951+17G>A MANE Select	ENSP00000207549.3:n.951+17G>A
ENST00000207549.8:c.951+17G>A	ENSP00000207549.3:n.951+17G>A
ENST00000412096.6:c.951+17G>A	ENSP00000388093.1:n.951+17G>A
ENST00000586147.1:c.118-3745G>A	ENSP00000466543.1:n.118-3745G>A
ENST00000587105.1:c.173+17G>A
ENST00000587504.5:n.954+17G>A
ENST00000591563.5:n.1163G>A
NM_199242.2:c.951+17G>A , LRG_122t1:c.951+17G>A	NP_954712.1:n.951+17G>A
XM_011524504.1:c.951+17G>A	XP_011522806.1:n.951+17G>A
XM_011524505.1:c.951+17G>A	XP_011522807.1:n.951+17G>A
XM_011524506.1:c.951+17G>A	XP_011522808.1:n.951+17G>A
XM_011524507.1:c.342+17G>A	XP_011522809.1:n.342+17G>A
XM_011524508.1:c.342+17G>A	XP_011522810.1:n.342+17G>A
XM_011524504.2:c.951+17G>A	XP_011522806.1:n.951+17G>A
XM_011524507.2:c.342+17G>A	XP_011522809.1:n.342+17G>A
XM_024450640.1:c.342+17G>A	XP_024306408.1:n.342+17G>A
NM_199242.3:c.951+17G>A MANE Select	NP_954712.1:n.951+17G>A