Canonical Allele Identifier: CA2677549377
Gene: GMNN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24777003_24777004insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG , CM000668.2:g.24777003_24777004insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG GRCh38
NC_000006.11:g.24777231_24777232insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG , CM000668.1:g.24777231_24777232insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG GRCh37
NC_000006.10:g.24885210_24885211insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG NCBI36
NG_030440.1:g.7073_7074insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000230056.8:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG MANE Select ENSP00000230056.3:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAA...
ENST00000230056.7:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG ENSP00000230056.3:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAA...
ENST00000356509.7:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG ENSP00000348902.3:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAA...
ENST00000378054.6:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG ENSP00000367293.2:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAA...
ENST00000378059.3:c.-244_-243insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG ENSP00000367298.3:n.-244_-243insCCCCTTTCTTCTCTTATGGTAAAGAACAA...
ENST00000468943.1:n.165-219_165-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG
ENST00000476555.5:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG ENSP00000419584.1:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAA...
ENST00000620958.4:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG ENSP00000477506.1:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAA...
NM_001251989.1:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG NP_001238918.1:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAA...
NM_001251990.1:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG NP_001238919.1:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAA...
NM_001251991.1:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG NP_001238920.1:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAA...
NM_015895.4:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG NP_056979.1:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAA...
XM_005249159.1:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG XP_005249216.1:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAA...
XM_005249159.2:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG XP_005249216.1:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAA...
NM_015895.5:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG MANE Select NP_056979.1:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAA...
NM_001251989.2:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG NP_001238918.1:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAA...
NM_001251990.2:c.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAACAAAG NP_001238919.1:n.-25-219_-25-218insCCCCTTTCTTCTCTTATGGTAAAGAA...