Canonical Allele Identifier: CA344255838

Gene: SYT2

Linked Data

• MyVariant Identifiers: chr1:g.202565982C>G (hg19) ; chr1:g.202596854C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596854C>G , CM000663.2:g.202596854C>G	GRCh38
NC_000001.10:g.202565982C>G , CM000663.1:g.202565982C>G	GRCh37
NC_000001.9:g.200832605C>G	NCBI36
NG_041776.1:g.118570G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1163G>C MANE Select	ENSP00000356237.4:p.Trp388Ser
ENST00000367267.5:c.1163G>C	ENSP00000356236.1:p.Trp388Ser
ENST00000367268.4:c.1163G>C	ENSP00000356237.4:p.Trp388Ser
NM_001136504.1:c.1163G>C	NP_001129976.1:p.Trp388Ser
NM_177402.4:c.1163G>C	NP_796376.2:p.Trp388Ser
XM_011509192.1:c.1172G>C	XP_011507494.1:p.Trp391Ser
XM_011509192.2:c.1172G>C	XP_011507494.1:p.Trp391Ser
XM_017000309.2:c.1343G>C	XP_016855798.1:p.Trp448Ser
XM_017000310.2:c.1334G>C	XP_016855799.1:p.Trp445Ser
XM_017000311.2:c.1172G>C	XP_016855800.1:p.Trp391Ser
XM_017000312.1:c.1172G>C	XP_016855801.1:p.Trp391Ser
XM_017000313.1:c.1163G>C	XP_016855802.1:p.Trp388Ser
NM_177402.5:c.1163G>C MANE Select	NP_796376.2:p.Trp388Ser