Canonical Allele Identifier: CA7222226

Gene: SYNE2 ESR2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64113367C>G , CM000676.2:g.64113367C>G	GRCh38
NC_000014.8:g.64580085C>G , CM000676.1:g.64580085C>G	GRCh37
NC_000014.7:g.63649838C>G	NCBI36
NG_011756.1:g.265403C>G
NG_011756.2:g.356469C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_182914.3:c.12636C>G (SYNE2) MANE Select	NP_878918.2:p.Asp4212Glu
ENST00000555002.6:c.12636C>G (SYNE2) MANE Select	ENSP00000450831.2:p.Asp4212Glu
NM_015180.4:c.12636C>G (SYNE2)	NP_055995.4:p.Asp4212Glu
NM_015180.5:c.12636C>G (SYNE2)	NP_055995.4:p.Asp4212Glu
NM_015180.6:c.12636C>G (SYNE2)	NP_055995.4:p.Asp4212Glu
NM_182914.2:c.12636C>G (SYNE2)	NP_878918.2:p.Asp4212Glu
ENST00000344113.8:c.12636C>G (SYNE2)	ENSP00000341781.4:p.Asp4212Glu
ENST00000357395.7:c.12681C>G (SYNE2)	ENSP00000349969.4:p.Asp4227Glu
ENST00000358025.7:c.12636C>G (SYNE2)	ENSP00000350719.3:p.Asp4212Glu
ENST00000394768.6:c.1791C>G (SYNE2)	ENSP00000378249.2:p.Asp597Glu
ENST00000553308.1:c.312C>G (SYNE2)	ENSP00000451520.1:p.Asp104Glu
ENST00000554584.5:c.12681C>G (SYNE2)	ENSP00000452570.1:p.Asp4227Glu
ENST00000555002.5:c.2538C>G (SYNE2)	ENSP00000450831.1:p.Asp846Glu
ENST00000556275.5:c.1407-28315G>C (ESR2)	ENSP00000452485.2:n.1407-28315G>C
ENST00000673797.1:c.39C>G (SYNE2)	ENSP00000501238.1:p.Asp13Glu
ENST00000673869.1:c.39C>G (SYNE2)	ENSP00000501077.1:p.Asp13Glu
XM_005267454.1:c.12636C>G (SYNE2)	XP_005267511.1:p.Asp4212Glu
XM_005267456.1:c.12636C>G (SYNE2)	XP_005267513.1:p.Asp4212Glu
XM_005267457.1:c.12636C>G (SYNE2)	XP_005267514.1:p.Asp4212Glu
XM_005267458.1:c.12636C>G (SYNE2)	XP_005267515.1:p.Asp4212Glu
XM_005267459.1:c.12636C>G (SYNE2)	XP_005267516.1:p.Asp4212Glu
XM_006720084.2:c.12636C>G (SYNE2)	XP_006720147.1:p.Asp4212Glu
XM_011536574.1:c.12636C>G (SYNE2)	XP_011534876.1:p.Asp4212Glu
XM_011536575.1:c.12636C>G (SYNE2)	XP_011534877.1:p.Asp4212Glu
XM_011536575.2:c.12636C>G (SYNE2)	XP_011534877.1:p.Asp4212Glu
XM_011536576.1:c.12636C>G (SYNE2)	XP_011534878.1:p.Asp4212Glu
XM_011536576.2:c.12636C>G (SYNE2)	XP_011534878.1:p.Asp4212Glu
XM_011536577.1:c.12636C>G (SYNE2)	XP_011534879.1:p.Asp4212Glu
XM_011536577.2:c.12636C>G (SYNE2)	XP_011534879.1:p.Asp4212Glu
XM_011536578.1:c.12636C>G (SYNE2)	XP_011534880.1:p.Asp4212Glu
XM_011536579.1:c.12636C>G (SYNE2)	XP_011534881.1:p.Asp4212Glu
XM_011536580.1:c.12636C>G (SYNE2)	XP_011534882.1:p.Asp4212Glu
XM_011536580.2:c.12636C>G (SYNE2)	XP_011534882.1:p.Asp4212Glu
XM_011536581.1:c.12636C>G (SYNE2)	XP_011534883.1:p.Asp4212Glu
XM_011536582.1:c.12519C>G (SYNE2)	XP_011534884.1:p.Asp4173Glu
XM_011536583.1:c.9441C>G (SYNE2)	XP_011534885.1:p.Asp3147Glu
XM_017021101.1:c.12636C>G (SYNE2)	XP_016876590.1:p.Asp4212Glu
XM_017021102.1:c.12567C>G (SYNE2)	XP_016876591.1:p.Asp4189Glu
XR_001750198.1:n.12866C>G (SYNE2)