Canonical Allele Identifier: CA2481403096
Gene: SYT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202596731_202596737delinsAGGTGTG , CM000663.2:g.202596731_202596737delinsAGGTGTG GRCh38
NC_000001.10:g.202565859_202565865delinsAGGTGTG , CM000663.1:g.202565859_202565865delinsAGGTGTG GRCh37
NC_000001.9:g.200832482_200832488delinsAGGTGTG NCBI36
NG_041776.1:g.118687_118693delinsCACACCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367268.5:c.*20_*26delinsCACACCT MANE Select ENSP00000356237.4:n.*20_*26delinsCACACCT
ENST00000367267.5:c.*20_*26delinsCACACCT ENSP00000356236.1:n.*20_*26delinsCACACCT
ENST00000367268.4:c.*20_*26delinsCACACCT ENSP00000356237.4:n.*20_*26delinsCACACCT
NM_001136504.1:c.*20_*26delinsCACACCT NP_001129976.1:n.*20_*26delinsCACACCT
NM_177402.4:c.*20_*26delinsCACACCT NP_796376.2:n.*20_*26delinsCACACCT
XM_011509192.1:c.*20_*26delinsCACACCT XP_011507494.1:n.*20_*26delinsCACACCT
XM_011509192.2:c.*20_*26delinsCACACCT XP_011507494.1:n.*20_*26delinsCACACCT
XM_017000309.2:c.*20_*26delinsCACACCT XP_016855798.1:n.*20_*26delinsCACACCT
XM_017000310.2:c.*20_*26delinsCACACCT XP_016855799.1:n.*20_*26delinsCACACCT
XM_017000311.2:c.*20_*26delinsCACACCT XP_016855800.1:n.*20_*26delinsCACACCT
XM_017000312.1:c.*20_*26delinsCACACCT XP_016855801.1:n.*20_*26delinsCACACCT
XM_017000313.1:c.*20_*26delinsCACACCT XP_016855802.1:n.*20_*26delinsCACACCT
NM_177402.5:c.*20_*26delinsCACACCT MANE Select NP_796376.2:n.*20_*26delinsCACACCT