Canonical Allele Identifier: CA587236239

Gene: UNC13B

Linked Data

• dbSNP Id: rs1250635771
• gnomAD v2: 9-35271732-CAT-C
• gnomAD v3: 9-35271735-CAT-C
• gnomAD v4: 9-35271735-CAT-C
• MyVariant Identifiers: chr9:g.35271733_35271734del (hg19) ; chr9:g.35271736_35271737del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35271736_35271737del , CM000671.2:g.35271736_35271737del	GRCh38
NC_000009.11:g.35271733_35271734del , CM000671.1:g.35271733_35271734del	GRCh37
NC_000009.10:g.35261733_35261734del	NCBI36
NG_033014.1:g.114745_114746del

Transcript Alleles

HGVS	Amino-acid change
ENST00000635942.2:c.526+12686_526+12687del MANE Select	ENSP00000490228.1:n.526+12686_526+12687del
ENST00000635942.1:c.526+12686_526+12687del	ENSP00000490228.1:n.526+12686_526+12687del
ENST00000378495.7:c.526+12686_526+12687del	ENSP00000367756.3:n.526+12686_526+12687del
ENST00000378496.8:c.-743+12686_-743+12687del	ENSP00000367757.5:n.-743+12686_-743+12687del
ENST00000396787.5:c.526+12686_526+12687del	ENSP00000380006.1:n.526+12686_526+12687del
ENST00000617908.4:c.-720+12686_-720+12687del	ENSP00000484432.1:n.-720+12686_-720+12687del
ENST00000619578.4:c.526+12686_526+12687del	ENSP00000479261.1:n.526+12686_526+12687del
ENST00000634487.1:c.526+12686_526+12687del	ENSP00000489581.1:n.526+12686_526+12687del
NM_006377.3:c.526+12686_526+12687del	NP_006368.3:n.526+12686_526+12687del
XM_011517684.1:c.526+12686_526+12687del	XP_011515986.1:n.526+12686_526+12687del
XM_011517685.1:c.526+12686_526+12687del	XP_011515987.1:n.526+12686_526+12687del
NM_001330653.1:c.526+12686_526+12687del	NP_001317582.1:n.526+12686_526+12687del
XM_011517685.3:c.526+12686_526+12687del	XP_011515987.1:n.526+12686_526+12687del
NM_001330653.2:c.526+12686_526+12687del	NP_001317582.1:n.526+12686_526+12687del
NM_001371186.1:c.526+12686_526+12687del	NP_001358115.1:n.526+12686_526+12687del
NM_001371189.1:c.526+12686_526+12687del	NP_001358118.1:n.526+12686_526+12687del
NM_006377.5:c.526+12686_526+12687del	NP_006368.3:n.526+12686_526+12687del
NM_001330653.3:c.526+12686_526+12687del	NP_001317582.1:n.526+12686_526+12687del
NM_001371186.2:c.526+12686_526+12687del	NP_001358115.1:n.526+12686_526+12687del
NM_001371189.2:c.526+12686_526+12687del MANE Select	NP_001358118.1:n.526+12686_526+12687del
NM_001387551.1:c.526+12686_526+12687del	NP_001374480.1:n.526+12686_526+12687del
NM_001387553.1:c.379+12686_379+12687del	NP_001374482.1:n.379+12686_379+12687del
NM_001387554.1:c.379+12686_379+12687del	NP_001374483.1:n.379+12686_379+12687del
NM_006377.6:c.526+12686_526+12687del	NP_006368.3:n.526+12686_526+12687del
NR_170667.1:n.801+12686_801+12687del