Canonical Allele Identifier: CA401108037

Gene: UNC13D

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75840100G>T , CM000679.2:g.75840100G>T	GRCh38
NC_000017.10:g.73836181G>T , CM000679.1:g.73836181G>T	GRCh37
NC_000017.9:g.71347776G>T	NCBI36
NG_007266.1:g.9618C>A , LRG_122:g.9618C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587504.6:c.850C>A	ENSP00000514388.1:p.Arg284=
ENST00000592386.6:c.851C>A	ENSP00000466826.2:p.Ser284Ter
ENST00000699511.1:c.49C>A
ENST00000207549.9:c.869C>A MANE Select	ENSP00000207549.3:p.Ser290Ter
ENST00000207549.8:c.869C>A	ENSP00000207549.3:p.Ser290Ter
ENST00000412096.6:c.869C>A	ENSP00000388093.1:p.Ser290Ter
ENST00000586147.1:c.118-3844C>A	ENSP00000466543.1:n.118-3844C>A
ENST00000587105.1:c.91C>A
ENST00000587504.5:n.872C>A
ENST00000591563.5:n.1064C>A
ENST00000592386.5:c.848C>A	ENSP00000466826.1:p.Ser283Ter
NM_199242.2:c.869C>A , LRG_122t1:c.869C>A	NP_954712.1:p.Ser290Ter
XM_011524504.1:c.869C>A	XP_011522806.1:p.Ser290Ter
XM_011524505.1:c.869C>A	XP_011522807.1:p.Ser290Ter
XM_011524506.1:c.869C>A	XP_011522808.1:p.Ser290Ter
XM_011524507.1:c.260C>A	XP_011522809.1:p.Ser87Ter
XM_011524508.1:c.260C>A	XP_011522810.1:p.Ser87Ter
XM_011524504.2:c.869C>A	XP_011522806.1:p.Ser290Ter
XM_011524507.2:c.260C>A	XP_011522809.1:p.Ser87Ter
XM_024450640.1:c.260C>A	XP_024306408.1:p.Ser87Ter
NM_199242.3:c.869C>A MANE Select	NP_954712.1:p.Ser290Ter