Canonical Allele Identifier: CA1190047220

Gene: SYT6

Linked Data

• dbSNP Id: rs2774307

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114128347A>C , CM000663.2:g.114128347A>C	GRCh38
NC_000001.10:g.114670969A>C , CM000663.1:g.114670969A>C	GRCh37
NC_000001.9:g.114472492A>C	NCBI36
NG_050730.1:g.30504T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369547.6:c.1071+9148T>G	ENSP00000358560.2:n.1071+9148T>G
ENST00000610222.3:c.1071+9148T>G MANE Select	ENSP00000476396.1:n.1071+9148T>G
ENST00000641643.2:c.816+9148T>G	ENSP00000493062.2:n.816+9148T>G
ENST00000369547.5:c.816+9148T>G	ENSP00000358560.1:n.816+9148T>G
ENST00000607941.5:c.816+9148T>G	ENSP00000476507.1:n.816+9148T>G
ENST00000609117.5:c.816+9148T>G	ENSP00000477344.1:n.816+9148T>G
ENST00000610096.1:c.*772+9148T>G	ENSP00000477325.1:n.*772+9148T>G
ENST00000610121.5:c.*772+9148T>G	ENSP00000476562.1:n.*772+9148T>G
ENST00000610222.1:c.1071+9148T>G	ENSP00000476396.1:n.1071+9148T>G
NM_001270805.1:c.816+9148T>G	NP_001257734.1:n.816+9148T>G
NM_205848.3:c.816+9148T>G	NP_995320.1:n.816+9148T>G
XM_011540751.1:c.816+9148T>G	XP_011539053.1:n.816+9148T>G
XR_946547.1:n.908+9148T>G
NM_001253772.2:c.1071+9148T>G MANE Select	NP_001240701.1:n.1071+9148T>G
NM_001366223.1:c.816+9148T>G	NP_001353152.1:n.816+9148T>G
NM_001366224.1:c.1071+9148T>G	NP_001353153.1:n.1071+9148T>G
NM_001366225.1:c.1071+9148T>G	NP_001353154.1:n.1071+9148T>G
NM_001366226.1:c.816+9148T>G	NP_001353155.1:n.816+9148T>G
XM_024453336.1:c.1032+9148T>G	XP_024309104.1:n.1032+9148T>G
XM_024453337.1:c.816+9148T>G	XP_024309105.1:n.816+9148T>G
XR_001736985.1:n.982+9148T>G
XR_002959489.1:n.2613+9148T>G
XR_946547.3:n.2613+9148T>G
NM_001270805.2:c.816+9148T>G	NP_001257734.1:n.816+9148T>G
NM_205848.4:c.816+9148T>G	NP_995320.1:n.816+9148T>G