Canonical Allele Identifier: CA1755358172

Gene: MNX1 MNX1-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157006467G= , CM000669.2:g.157006467G=	GRCh38
NC_000007.13:g.156799161G= , CM000669.1:g.156799161G=	GRCh37
NC_000007.12:g.156491922G=	NCBI36
NG_013212.1:g.9187C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252971.11:c.852+12C= (MNX1) MANE Select	ENSP00000252971.5:n.852+12C=
ENST00000252971.10:c.852+12C= (MNX1)	ENSP00000252971.5:n.852+12C=
ENST00000425745.1:c.56-594C= (MNX1)	ENSP00000416458.1:n.56-594C=
ENST00000428439.1:c.216+12C= (MNX1)	ENSP00000401158.1:n.216+12C=
ENST00000469500.5:c.55+2531C= (MNX1)	ENSP00000475129.1:n.55+2531C=
ENST00000474448.1:c.*254+12C= (MNX1)	ENSP00000473965.1:n.*254+12C=
ENST00000479817.1:c.38+3193C= (MNX1)
ENST00000543409.5:c.216+12C= (MNX1)	ENSP00000438552.1:n.216+12C=
NM_001165255.1:c.216+12C= (MNX1)	NP_001158727.1:n.216+12C=
NM_005515.3:c.852+12C= (MNX1)	NP_005506.3:n.852+12C=
XR_928257.1:n.544+43G= (MNX1-AS2)
NR_147077.1:n.118+43G= (MNX1-AS2)
NM_005515.4:c.852+12C= (MNX1) MANE Select	NP_005506.3:n.852+12C=
NM_001165255.2:c.216+12C= (MNX1)	NP_001158727.1:n.216+12C=