Canonical Allele Identifier: CA2695208863

Gene: MNX1 MNX1-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157006555_157006557delinsCCAGCTCCAGCAGCTCCA , CM000669.2:g.157006555_157006557delinsCCAGCTCCAGCAGCTCCA	GRCh38
NC_000007.13:g.156799249_156799251delinsCCAGCTCCAGCAGCTCCA , CM000669.1:g.156799249_156799251delinsCCAGCTCCAGCAGCTCCA	GRCh37
NC_000007.12:g.156492010_156492012delinsCCAGCTCCAGCAGCTCCA	NCBI36
NG_013212.1:g.9097_9099delinsTGGAGCTGCTGGAGCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252971.11:c.774_776delinsTGGAGCTGCTGGAGCTGG (MNX1) MANE Select	ENSP00000252971.5:p.Gln259delinsGlyAlaAlaGlyAlaGly
ENST00000252971.10:c.774_776delinsTGGAGCTGCTGGAGCTGG (MNX1)	ENSP00000252971.5:p.Gln259delinsGlyAlaAlaGlyAlaGly
ENST00000425745.1:c.56-684_56-682delinsTGGAGCTGCTGGAGCTGG (MNX1)	ENSP00000416458.1:n.56-684_56-682delinsTGGAGCTGCTGGAGCTGG
ENST00000428439.1:c.138_140delinsTGGAGCTGCTGGAGCTGG (MNX1)	ENSP00000401158.1:p.Gln47delinsGlyAlaAlaGlyAlaGly
ENST00000469500.5:c.55+2441_55+2443delinsTGGAGCTGCTGGAGCTGG (MNX1)	ENSP00000475129.1:n.55+2441_55+2443delinsTGGAGCTGCTGGAGCTGG
ENST00000474448.1:c.*176_*178delinsTGGAGCTGCTGGAGCTGG (MNX1)	ENSP00000473965.1:n.*176_*178delinsTGGAGCTGCTGGAGCTGG
ENST00000479817.1:c.38+3103_38+3105delinsTGGAGCTGCTGGAGCTGG (MNX1)
ENST00000543409.5:c.138_140delinsTGGAGCTGCTGGAGCTGG (MNX1)	ENSP00000438552.1:p.Gln47delinsGlyAlaAlaGlyAlaGly
NM_001165255.1:c.138_140delinsTGGAGCTGCTGGAGCTGG (MNX1)	NP_001158727.1:p.Gln47delinsGlyAlaAlaGlyAlaGly
NM_005515.3:c.774_776delinsTGGAGCTGCTGGAGCTGG (MNX1)	NP_005506.3:p.Gln259delinsGlyAlaAlaGlyAlaGly
XR_928257.1:n.544+131_544+133delinsCCAGCTCCAGCAGCTCCA (MNX1-AS2)
NR_147077.1:n.118+131_118+133delinsCCAGCTCCAGCAGCTCCA (MNX1-AS2)
NM_005515.4:c.774_776delinsTGGAGCTGCTGGAGCTGG (MNX1) MANE Select	NP_005506.3:p.Gln259delinsGlyAlaAlaGlyAlaGly
NM_001165255.2:c.138_140delinsTGGAGCTGCTGGAGCTGG (MNX1)	NP_001158727.1:p.Gln47delinsGlyAlaAlaGlyAlaGly