Canonical Allele Identifier: CA401098928

Gene: UNC13D

Linked Data

• MyVariant Identifiers: chr17:g.73832328T>C (hg19) ; chr17:g.75836247T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75836247T>C , CM000679.2:g.75836247T>C	GRCh38
NC_000017.10:g.73832328T>C , CM000679.1:g.73832328T>C	GRCh37
NC_000017.9:g.71343923T>C	NCBI36
NG_007266.1:g.13471A>G , LRG_122:g.13471A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000699510.1:c.334A>G	ENSP00000514405.1:p.Thr112Ala
ENST00000699511.1:c.576A>G
ENST00000207549.9:c.1399A>G MANE Select	ENSP00000207549.3:p.Thr467Ala
ENST00000207549.8:c.1399A>G	ENSP00000207549.3:p.Thr467Ala
ENST00000412096.6:c.1399A>G	ENSP00000388093.1:p.Thr467Ala
ENST00000586147.1:c.127A>G	ENSP00000466543.1:p.Thr43Ala
ENST00000587105.1:c.518A>G
ENST00000591563.5:n.1669A>G
NM_199242.2:c.1399A>G , LRG_122t1:c.1399A>G	NP_954712.1:p.Thr467Ala
XM_011524504.1:c.1399A>G	XP_011522806.1:p.Thr467Ala
XM_011524505.1:c.1399A>G	XP_011522807.1:p.Thr467Ala
XM_011524506.1:c.1396A>G	XP_011522808.1:p.Thr466Ala
XM_011524507.1:c.790A>G	XP_011522809.1:p.Thr264Ala
XM_011524508.1:c.790A>G	XP_011522810.1:p.Thr264Ala
XM_011524504.2:c.1399A>G	XP_011522806.1:p.Thr467Ala
XM_011524507.2:c.790A>G	XP_011522809.1:p.Thr264Ala
XM_024450640.1:c.790A>G	XP_024306408.1:p.Thr264Ala
NM_199242.3:c.1399A>G MANE Select	NP_954712.1:p.Thr467Ala