Canonical Allele Identifier: CA370162328

Gene: MNX1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157005875T>C , CM000669.2:g.157005875T>C	GRCh38
NC_000007.13:g.156798569T>C , CM000669.1:g.156798569T>C	GRCh37
NC_000007.12:g.156491330T>C	NCBI36
NG_013212.1:g.9779A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252971.11:c.853-2A>G MANE Select	ENSP00000252971.5:n.853-2A>G
ENST00000252971.10:c.853-2A>G	ENSP00000252971.5:n.853-2A>G
ENST00000425745.1:c.56-2A>G	ENSP00000416458.1:n.56-2A>G
ENST00000428439.1:c.217-2A>G	ENSP00000401158.1:n.217-2A>G
ENST00000469500.5:c.55+3123A>G	ENSP00000475129.1:n.55+3123A>G
ENST00000474448.1:c.*255-2A>G	ENSP00000473965.1:n.*255-2A>G
ENST00000479817.1:c.38+3785A>G
ENST00000543409.5:c.217-2A>G	ENSP00000438552.1:n.217-2A>G
NM_001165255.1:c.217-2A>G	NP_001158727.1:n.217-2A>G
NM_005515.3:c.853-2A>G	NP_005506.3:n.853-2A>G
NM_005515.4:c.853-2A>G MANE Select	NP_005506.3:n.853-2A>G
NM_001165255.2:c.217-2A>G	NP_001158727.1:n.217-2A>G