Canonical Allele Identifier: CA402858602

Gene: MIER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.336150A>C , CM000681.2:g.336150A>C	GRCh38
NC_000019.9:g.336150A>C , CM000681.1:g.336150A>C	GRCh37
NC_000019.8:g.287150A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017550.3:c.33T>G MANE Select	NP_060020.1:p.Ser11Arg
ENST00000264819.7:c.33T>G MANE Select	ENSP00000264819.3:p.Ser11Arg
NM_001346105.1:c.-8-1608T>G	NP_001333034.1:n.-8-1608T>G
NM_001346105.2:c.-8-1608T>G	NP_001333034.1:n.-8-1608T>G
NM_001387152.1:c.39T>G	NP_001374081.1:p.Ser13Arg
NM_001387153.1:c.33T>G	NP_001374082.1:p.Ser11Arg
NM_001387154.1:c.-8-1608T>G	NP_001374083.1:n.-8-1608T>G
NM_001387155.1:c.-76T>G	NP_001374084.1:n.-76T>G
NM_001387156.1:c.-337T>G	NP_001374085.1:n.-337T>G
NM_001387157.1:c.-269-1608T>G	NP_001374086.1:n.-269-1608T>G
NM_017550.1:c.33T>G	NP_060020.1:p.Ser11Arg
NM_017550.2:c.33T>G	NP_060020.1:p.Ser11Arg
ENST00000264819.6:c.33T>G	ENSP00000264819.3:p.Ser11Arg
ENST00000586994.7:n.29T>G
ENST00000587966.2:n.35-1608T>G
ENST00000592722.1:n.110T>G
ENST00000621180.4:n.45T>G
ENST00000635755.1:c.10-1608T>G	ENSP00000490045.1:n.10-1608T>G
XM_005259582.3:c.39T>G	XP_005259639.1:p.Ser13Arg
XM_005259582.5:c.39T>G	XP_005259639.1:p.Ser13Arg
XM_006722769.2:c.39T>G	XP_006722832.1:p.Ser13Arg
XM_006722769.4:c.39T>G	XP_006722832.1:p.Ser13Arg
XM_011528072.1:c.39T>G	XP_011526374.1:p.Ser13Arg
XM_011528073.1:c.33T>G	XP_011526375.1:p.Ser11Arg
XM_011528074.1:c.39T>G	XP_011526376.1:p.Ser13Arg
XM_011528075.1:c.-76T>G	XP_011526377.1:n.-76T>G
XM_011528076.1:c.-76T>G	XP_011526378.1:n.-76T>G
XM_011528077.1:c.-76T>G	XP_011526379.1:n.-76T>G
XM_011528078.1:c.-76T>G	XP_011526380.1:n.-76T>G
XM_011528079.1:c.-76T>G	XP_011526381.1:n.-76T>G
XM_011528080.1:c.-8-1608T>G	XP_011526382.1:n.-8-1608T>G
XM_024451548.1:c.-76T>G	XP_024307316.1:n.-76T>G
XM_024451549.1:c.-76T>G	XP_024307317.1:n.-76T>G
XM_024451550.1:c.-76T>G	XP_024307318.1:n.-76T>G