Canonical Allele Identifier: CA344255765

Gene: SYT2

Linked Data

• MyVariant Identifiers: chr1:g.202565947C>G (hg19) ; chr1:g.202596819C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596819C>G , CM000663.2:g.202596819C>G	GRCh38
NC_000001.10:g.202565947C>G , CM000663.1:g.202565947C>G	GRCh37
NC_000001.9:g.200832570C>G	NCBI36
NG_041776.1:g.118605G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1198G>C MANE Select	ENSP00000356237.4:p.Ala400Pro
ENST00000367267.5:c.1198G>C	ENSP00000356236.1:p.Ala400Pro
ENST00000367268.4:c.1198G>C	ENSP00000356237.4:p.Ala400Pro
NM_001136504.1:c.1198G>C	NP_001129976.1:p.Ala400Pro
NM_177402.4:c.1198G>C	NP_796376.2:p.Ala400Pro
XM_011509192.1:c.1207G>C	XP_011507494.1:p.Ala403Pro
XM_011509192.2:c.1207G>C	XP_011507494.1:p.Ala403Pro
XM_017000309.2:c.1378G>C	XP_016855798.1:p.Ala460Pro
XM_017000310.2:c.1369G>C	XP_016855799.1:p.Ala457Pro
XM_017000311.2:c.1207G>C	XP_016855800.1:p.Ala403Pro
XM_017000312.1:c.1207G>C	XP_016855801.1:p.Ala403Pro
XM_017000313.1:c.1198G>C	XP_016855802.1:p.Ala400Pro
NM_177402.5:c.1198G>C MANE Select	NP_796376.2:p.Ala400Pro