Canonical Allele Identifier: CA7223020

Gene: SYNE2 ESR2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64142000A>G , CM000676.2:g.64142000A>G	GRCh38
NC_000014.8:g.64608718A>G , CM000676.1:g.64608718A>G	GRCh37
NC_000014.7:g.63678471A>G	NCBI36
NG_011756.1:g.294036A>G
NG_011756.2:g.385102A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_182914.3:c.15218A>G (SYNE2) MANE Select	NP_878918.2:p.Asn5073Ser
ENST00000555002.6:c.15218A>G (SYNE2) MANE Select	ENSP00000450831.2:p.Asn5073Ser
NM_015180.4:c.15218A>G (SYNE2)	NP_055995.4:p.Asn5073Ser
NM_015180.5:c.15218A>G (SYNE2)	NP_055995.4:p.Asn5073Ser
NM_015180.6:c.15218A>G (SYNE2)	NP_055995.4:p.Asn5073Ser
NM_182914.2:c.15218A>G (SYNE2)	NP_878918.2:p.Asn5073Ser
ENST00000344113.8:c.15218A>G (SYNE2)	ENSP00000341781.4:p.Asn5073Ser
ENST00000357395.7:c.14987A>G (SYNE2)	ENSP00000349969.4:p.Asn4996Ser
ENST00000358025.7:c.15218A>G (SYNE2)	ENSP00000350719.3:p.Asn5073Ser
ENST00000394768.6:c.4373A>G (SYNE2)	ENSP00000378249.2:p.Asn1458Ser
ENST00000554584.5:c.14969A>G (SYNE2)	ENSP00000452570.1:p.Asn4990Ser
ENST00000555002.5:c.5120A>G (SYNE2)	ENSP00000450831.1:p.Asn1707Ser
ENST00000555612.5:c.104A>G (SYNE2)	ENSP00000451972.1:p.Asn35Ser
ENST00000556275.5:c.1407-56948T>C (ESR2)	ENSP00000452485.2:n.1407-56948T>C
XM_005267454.1:c.15218A>G (SYNE2)	XP_005267511.1:p.Asn5073Ser
XM_005267456.1:c.15218A>G (SYNE2)	XP_005267513.1:p.Asn5073Ser
XM_005267457.1:c.15218A>G (SYNE2)	XP_005267514.1:p.Asn5073Ser
XM_005267458.1:c.15218A>G (SYNE2)	XP_005267515.1:p.Asn5073Ser
XM_005267459.1:c.15218A>G (SYNE2)	XP_005267516.1:p.Asn5073Ser
XM_011536574.1:c.15218A>G (SYNE2)	XP_011534876.1:p.Asn5073Ser
XM_011536575.1:c.15218A>G (SYNE2)	XP_011534877.1:p.Asn5073Ser
XM_011536575.2:c.15218A>G (SYNE2)	XP_011534877.1:p.Asn5073Ser
XM_011536576.1:c.15218A>G (SYNE2)	XP_011534878.1:p.Asn5073Ser
XM_011536576.2:c.15218A>G (SYNE2)	XP_011534878.1:p.Asn5073Ser
XM_011536577.1:c.15218A>G (SYNE2)	XP_011534879.1:p.Asn5073Ser
XM_011536577.2:c.15218A>G (SYNE2)	XP_011534879.1:p.Asn5073Ser
XM_011536578.1:c.15218A>G (SYNE2)	XP_011534880.1:p.Asn5073Ser
XM_011536579.1:c.15218A>G (SYNE2)	XP_011534881.1:p.Asn5073Ser
XM_011536580.1:c.15218A>G (SYNE2)	XP_011534882.1:p.Asn5073Ser
XM_011536580.2:c.15218A>G (SYNE2)	XP_011534882.1:p.Asn5073Ser
XM_011536581.1:c.15218A>G (SYNE2)	XP_011534883.1:p.Asn5073Ser
XM_011536582.1:c.15101A>G (SYNE2)	XP_011534884.1:p.Asn5034Ser
XM_011536583.1:c.12023A>G (SYNE2)	XP_011534885.1:p.Asn4008Ser
XM_017021101.1:c.15218A>G (SYNE2)	XP_016876590.1:p.Asn5073Ser
XM_017021102.1:c.15149A>G (SYNE2)	XP_016876591.1:p.Asn5050Ser