Canonical Allele Identifier: CA8772379

Gene: UNC13D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75830364T>C , CM000679.2:g.75830364T>C	GRCh38
NC_000017.10:g.73826445T>C , CM000679.1:g.73826445T>C	GRCh37
NC_000017.9:g.71338040T>C	NCBI36
NG_007266.1:g.19354A>G , LRG_122:g.19354A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_199242.3:c.2828A>G MANE Select	NP_954712.1:p.Asn943Ser
ENST00000207549.9:c.2828A>G MANE Select	ENSP00000207549.3:p.Asn943Ser
NM_199242.2:c.2828A>G , LRG_122t1:c.2828A>G	NP_954712.1:p.Asn943Ser
ENST00000207549.8:c.2828A>G	ENSP00000207549.3:p.Asn943Ser
ENST00000412096.6:c.2828A>G	ENSP00000388093.1:p.Asn943Ser
ENST00000586519.1:c.74A>G	ENSP00000466149.1:p.Asn25Ser
ENST00000590856.1:n.203A>G
ENST00000699510.1:c.1694A>G	ENSP00000514405.1:p.Asn565Ser
XM_011524504.1:c.2897A>G	XP_011522806.1:p.Asn966Ser
XM_011524504.2:c.2897A>G	XP_011522806.1:p.Asn966Ser
XM_011524505.1:c.2897A>G	XP_011522807.1:p.Asn966Ser
XM_011524506.1:c.2894A>G	XP_011522808.1:p.Asn965Ser
XM_011524507.1:c.2288A>G	XP_011522809.1:p.Asn763Ser
XM_011524507.2:c.2288A>G	XP_011522809.1:p.Asn763Ser
XM_011524508.1:c.2288A>G	XP_011522810.1:p.Asn763Ser
XM_024450640.1:c.2288A>G	XP_024306408.1:p.Asn763Ser