Canonical Allele Identifier: CA8773167

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75839880G>A , CM000679.2:g.75839880G>A	GRCh38
NC_000017.10:g.73835961G>A , CM000679.1:g.73835961G>A	GRCh37
NC_000017.9:g.71347556G>A	NCBI36
NG_007266.1:g.9838C>T , LRG_122:g.9838C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.1014C>T MANE Select	NP_954712.1:p.His338=
ENST00000207549.9:c.1014C>T MANE Select	ENSP00000207549.3:p.His338=
NM_199242.2:c.1014C>T , LRG_122t1:c.1014C>T	NP_954712.1:p.His338=
ENST00000207549.8:c.1014C>T	ENSP00000207549.3:p.His338=
ENST00000412096.6:c.1014C>T	ENSP00000388093.1:p.His338=
ENST00000586147.1:c.118-3624C>T	ENSP00000466543.1:n.118-3624C>T
ENST00000587105.1:c.236C>T
ENST00000587504.5:n.1017C>T
ENST00000587504.6:c.*32C>T	ENSP00000514388.1:n.*32C>T
ENST00000591563.5:n.1284C>T
ENST00000699511.1:c.194C>T
XM_011524504.1:c.1014C>T	XP_011522806.1:p.His338=
XM_011524504.2:c.1014C>T	XP_011522806.1:p.His338=
XM_011524505.1:c.1014C>T	XP_011522807.1:p.His338=
XM_011524506.1:c.1014C>T	XP_011522808.1:p.His338=
XM_011524507.1:c.405C>T	XP_011522809.1:p.His135=
XM_011524507.2:c.405C>T	XP_011522809.1:p.His135=
XM_011524508.1:c.405C>T	XP_011522810.1:p.His135=
XM_024450640.1:c.405C>T	XP_024306408.1:p.His135=