Canonical Allele Identifier: CA2685830266

Gene: MNX1 MNX1-AS2

Linked Data

• gnomAD v4: 7-157006466-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157006466G>A , CM000669.2:g.157006466G>A	GRCh38
NC_000007.13:g.156799160G>A , CM000669.1:g.156799160G>A	GRCh37
NC_000007.12:g.156491921G>A	NCBI36
NG_013212.1:g.9188C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252971.11:c.852+13C>T (MNX1) MANE Select	ENSP00000252971.5:n.852+13C>T
ENST00000252971.10:c.852+13C>T (MNX1)	ENSP00000252971.5:n.852+13C>T
ENST00000425745.1:c.56-593C>T (MNX1)	ENSP00000416458.1:n.56-593C>T
ENST00000428439.1:c.216+13C>T (MNX1)	ENSP00000401158.1:n.216+13C>T
ENST00000469500.5:c.55+2532C>T (MNX1)	ENSP00000475129.1:n.55+2532C>T
ENST00000474448.1:c.*254+13C>T (MNX1)	ENSP00000473965.1:n.*254+13C>T
ENST00000479817.1:c.38+3194C>T (MNX1)
ENST00000543409.5:c.216+13C>T (MNX1)	ENSP00000438552.1:n.216+13C>T
NM_001165255.1:c.216+13C>T (MNX1)	NP_001158727.1:n.216+13C>T
NM_005515.3:c.852+13C>T (MNX1)	NP_005506.3:n.852+13C>T
XR_928257.1:n.544+42G>A (MNX1-AS2)
NR_147077.1:n.118+42G>A (MNX1-AS2)
NM_005515.4:c.852+13C>T (MNX1) MANE Select	NP_005506.3:n.852+13C>T
NM_001165255.2:c.216+13C>T (MNX1)	NP_001158727.1:n.216+13C>T