Canonical Allele Identifier: CA775103846

Gene: UNC13D

Linked Data

• dbSNP Id: rs759694327
• gnomAD v4: 17-75835563-T-TG
• MyVariant Identifiers: chr17:g.73831644_73831645insG (hg19) ; chr17:g.75835563_75835564insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75835567dup , CM000679.2:g.75835567dup	GRCh38
NC_000017.10:g.73831648dup , CM000679.1:g.73831648dup	GRCh37
NC_000017.9:g.71343243dup	NCBI36
NG_007266.1:g.14154dup , LRG_122:g.14154dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000699510.1:c.663-35dup	ENSP00000514405.1:n.663-35dup
ENST00000207549.9:c.1728-35dup MANE Select	ENSP00000207549.3:n.1728-35dup
ENST00000207549.8:c.1728-35dup	ENSP00000207549.3:n.1728-35dup
ENST00000412096.6:c.1728-35dup	ENSP00000388093.1:n.1728-35dup
ENST00000586147.1:c.456-35dup	ENSP00000466543.1:n.456-35dup
ENST00000591563.5:n.1998-35dup
NM_199242.2:c.1728-35dup , LRG_122t1:c.1728-35dup	NP_954712.1:n.1728-35dup
XM_011524504.1:c.1728-35dup	XP_011522806.1:n.1728-35dup
XM_011524505.1:c.1728-35dup	XP_011522807.1:n.1728-35dup
XM_011524506.1:c.1725-35dup	XP_011522808.1:n.1725-35dup
XM_011524507.1:c.1119-35dup	XP_011522809.1:n.1119-35dup
XM_011524508.1:c.1119-35dup	XP_011522810.1:n.1119-35dup
XM_011524504.2:c.1728-35dup	XP_011522806.1:n.1728-35dup
XM_011524507.2:c.1119-35dup	XP_011522809.1:n.1119-35dup
XM_024450640.1:c.1119-35dup	XP_024306408.1:n.1119-35dup
NM_199242.3:c.1728-35dup MANE Select	NP_954712.1:n.1728-35dup