Canonical Allele Identifier: CA10640577

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75828797G>T , CM000679.2:g.75828797G>T	GRCh38
NC_000017.10:g.73824878G>T , CM000679.1:g.73824878G>T	GRCh37
NC_000017.9:g.71336473G>T	NCBI36
NG_007266.1:g.20921C>A , LRG_122:g.20921C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.3141C>A MANE Select	NP_954712.1:p.Pro1047=
ENST00000207549.9:c.3141C>A MANE Select	ENSP00000207549.3:p.Pro1047=
NM_199242.2:c.3141C>A , LRG_122t1:c.3141C>A	NP_954712.1:p.Pro1047=
ENST00000207549.8:c.3141C>A	ENSP00000207549.3:p.Pro1047=
ENST00000412096.6:c.3141C>A	ENSP00000388093.1:p.Pro1047=
ENST00000586519.1:c.263C>A	ENSP00000466149.1:n.263C>A
ENST00000589670.5:c.307C>A
ENST00000699510.1:c.2007C>A	ENSP00000514405.1:p.Pro669=
XM_011524504.1:c.3210C>A	XP_011522806.1:p.Pro1070=
XM_011524504.2:c.3210C>A	XP_011522806.1:p.Pro1070=
XM_011524505.1:c.3210C>A	XP_011522807.1:p.Pro1070=
XM_011524506.1:c.3207C>A	XP_011522808.1:p.Pro1069=
XM_011524507.1:c.2601C>A	XP_011522809.1:p.Pro867=
XM_011524507.2:c.2601C>A	XP_011522809.1:p.Pro867=
XM_011524508.1:c.2601C>A	XP_011522810.1:p.Pro867=
XM_024450640.1:c.2601C>A	XP_024306408.1:p.Pro867=