Canonical Allele Identifier: CA344255858

Gene: SYT2

Linked Data

• MyVariant Identifiers: chr1:g.202565991A>T (hg19) ; chr1:g.202596863A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596863A>T , CM000663.2:g.202596863A>T	GRCh38
NC_000001.10:g.202565991A>T , CM000663.1:g.202565991A>T	GRCh37
NC_000001.9:g.200832614A>T	NCBI36
NG_041776.1:g.118561T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1154T>A MANE Select	ENSP00000356237.4:p.Leu385Gln
ENST00000367267.5:c.1154T>A	ENSP00000356236.1:p.Leu385Gln
ENST00000367268.4:c.1154T>A	ENSP00000356237.4:p.Leu385Gln
NM_001136504.1:c.1154T>A	NP_001129976.1:p.Leu385Gln
NM_177402.4:c.1154T>A	NP_796376.2:p.Leu385Gln
XM_011509192.1:c.1163T>A	XP_011507494.1:p.Leu388Gln
XM_011509192.2:c.1163T>A	XP_011507494.1:p.Leu388Gln
XM_017000309.2:c.1334T>A	XP_016855798.1:p.Leu445Gln
XM_017000310.2:c.1325T>A	XP_016855799.1:p.Leu442Gln
XM_017000311.2:c.1163T>A	XP_016855800.1:p.Leu388Gln
XM_017000312.1:c.1163T>A	XP_016855801.1:p.Leu388Gln
XM_017000313.1:c.1154T>A	XP_016855802.1:p.Leu385Gln
NM_177402.5:c.1154T>A MANE Select	NP_796376.2:p.Leu385Gln