Canonical Allele Identifier: CA7223359
Community Standard Title: NM_182914.3(SYNE2):c.16374A>T (p.Gln5458His)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64163476A>T , CM000676.2:g.64163476A>T GRCh38
NC_000014.8:g.64630194A>T , CM000676.1:g.64630194A>T GRCh37
NC_000014.7:g.63699947A>T NCBI36
NG_011756.1:g.315512A>T
NG_011756.2:g.406578A>T

Transcript Alleles

HGVS Amino-acid Change
NM_182914.3:c.16374A>T (SYNE2) MANE Select NP_878918.2:p.Gln5458His
ENST00000555002.6:c.16374A>T (SYNE2) MANE Select ENSP00000450831.2:p.Gln5458His
NM_015180.4:c.16374A>T (SYNE2) NP_055995.4:p.Gln5458His
NM_015180.5:c.16374A>T (SYNE2) NP_055995.4:p.Gln5458His
NM_015180.6:c.16374A>T (SYNE2) NP_055995.4:p.Gln5458His
NM_182914.2:c.16374A>T (SYNE2) NP_878918.2:p.Gln5458His
ENST00000344113.8:c.16374A>T (SYNE2) ENSP00000341781.4:p.Gln5458His
ENST00000357395.7:c.16143A>T (SYNE2) ENSP00000349969.4:p.Gln5381His
ENST00000358025.7:c.16374A>T (SYNE2) ENSP00000350719.3:p.Gln5458His
ENST00000394768.6:c.5529A>T (SYNE2) ENSP00000378249.2:p.Gln1843His
ENST00000553289.5:c.129A>T (SYNE2) ENSP00000451184.1:p.Gln43His
ENST00000554584.5:c.16125A>T (SYNE2) ENSP00000452570.1:p.Gln5375His
ENST00000555002.5:c.6276A>T (SYNE2) ENSP00000450831.1:p.Gln2092His
ENST00000555612.5:c.1260A>T (SYNE2) ENSP00000451972.1:p.Gln420His
ENST00000556275.5:c.1406+71494T>A (ESR2) ENSP00000452485.2:n.1406+71494T>A
XM_005267454.1:c.16374A>T (SYNE2) XP_005267511.1:p.Gln5458His
XM_005267456.1:c.16374A>T (SYNE2) XP_005267513.1:p.Gln5458His
XM_005267457.1:c.16374A>T (SYNE2) XP_005267514.1:p.Gln5458His
XM_005267458.1:c.16374A>T (SYNE2) XP_005267515.1:p.Gln5458His
XM_005267459.1:c.16374A>T (SYNE2) XP_005267516.1:p.Gln5458His
XM_011536574.1:c.16374A>T (SYNE2) XP_011534876.1:p.Gln5458His
XM_011536575.1:c.16374A>T (SYNE2) XP_011534877.1:p.Gln5458His
XM_011536575.2:c.16374A>T (SYNE2) XP_011534877.1:p.Gln5458His
XM_011536576.1:c.16374A>T (SYNE2) XP_011534878.1:p.Gln5458His
XM_011536576.2:c.16374A>T (SYNE2) XP_011534878.1:p.Gln5458His
XM_011536577.1:c.16374A>T (SYNE2) XP_011534879.1:p.Gln5458His
XM_011536577.2:c.16374A>T (SYNE2) XP_011534879.1:p.Gln5458His
XM_011536578.1:c.16374A>T (SYNE2) XP_011534880.1:p.Gln5458His
XM_011536579.1:c.16374A>T (SYNE2) XP_011534881.1:p.Gln5458His
XM_011536580.1:c.16374A>T (SYNE2) XP_011534882.1:p.Gln5458His
XM_011536580.2:c.16374A>T (SYNE2) XP_011534882.1:p.Gln5458His
XM_011536581.1:c.16374A>T (SYNE2) XP_011534883.1:p.Gln5458His
XM_011536582.1:c.16257A>T (SYNE2) XP_011534884.1:p.Gln5419His
XM_011536583.1:c.13179A>T (SYNE2) XP_011534885.1:p.Gln4393His
XM_017021101.1:c.16374A>T (SYNE2) XP_016876590.1:p.Gln5458His
XM_017021102.1:c.16305A>T (SYNE2) XP_016876591.1:p.Gln5435His