Canonical Allele Identifier: CA14637712

Gene: UNC13A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17641880A>C , CM000681.2:g.17641880A>C	GRCh38
NC_000019.9:g.17752689A>C , CM000681.1:g.17752689A>C	GRCh37
NC_000019.8:g.17613689A>C	NCBI36
NG_052872.1:g.51465T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519716.7:c.2473-324T>G MANE Select	ENSP00000429562.2:n.2473-324T>G
ENST00000252773.11:c.2473-324T>G	ENSP00000252773.8:n.2473-324T>G
ENST00000519716.6:c.2473-324T>G	ENSP00000429562.2:n.2473-324T>G
ENST00000550896.1:c.2467-324T>G	ENSP00000446831.1:n.2467-324T>G
ENST00000551649.5:c.2473-324T>G	ENSP00000447236.1:n.2473-324T>G
ENST00000552293.5:c.2473-324T>G	ENSP00000447572.1:n.2473-324T>G
NM_001080421.2:c.2473-324T>G	NP_001073890.2:n.2473-324T>G
XM_011527809.1:c.2467-324T>G	XP_011526111.1:n.2467-324T>G
XM_011527810.1:c.2443-324T>G	XP_011526112.1:n.2443-324T>G
XM_011527811.1:c.2473-324T>G	XP_011526113.1:n.2473-324T>G
XM_011527812.1:c.1714-324T>G	XP_011526114.1:n.1714-324T>G
XM_011527813.1:c.2467-324T>G	XP_011526115.1:n.2467-324T>G
XM_011527810.2:c.2443-324T>G	XP_011526112.1:n.2443-324T>G
XM_011527811.2:c.2473-324T>G	XP_011526113.1:n.2473-324T>G
XM_017026502.1:c.2473-324T>G	XP_016881991.1:n.2473-324T>G
NM_001080421.3:c.2473-324T>G MANE Select	NP_001073890.2:n.2473-324T>G
NM_001387021.1:c.2467-324T>G	NP_001373950.1:n.2467-324T>G
NM_001387022.1:c.2467-324T>G	NP_001373951.1:n.2467-324T>G
NM_001387023.1:c.2467-324T>G	NP_001373952.1:n.2467-324T>G