Canonical Allele Identifier: CA2677549790

Gene: GMNN

Linked Data

• gnomAD v4: 6-24777581-C-CAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24777581_24777582insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA , CM000668.2:g.24777581_24777582insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	GRCh38
NC_000006.11:g.24777809_24777810insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA , CM000668.1:g.24777809_24777810insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	GRCh37
NC_000006.10:g.24885788_24885789insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	NCBI36
NG_030440.1:g.7651_7652insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230056.8:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA MANE Select	ENSP00000230056.3:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTG...
ENST00000230056.7:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	ENSP00000230056.3:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTG...
ENST00000356509.7:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	ENSP00000348902.3:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTG...
ENST00000378054.6:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	ENSP00000367293.2:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTG...
ENST00000378059.3:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	ENSP00000367298.3:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTG...
ENST00000468943.1:n.524_525insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA
ENST00000476555.5:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	ENSP00000419584.1:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTG...
ENST00000620958.4:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	ENSP00000477506.1:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTG...
NM_001251989.1:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	NP_001238918.1:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAA...
NM_001251990.1:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	NP_001238919.1:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAA...
NM_001251991.1:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	NP_001238920.1:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAA...
NM_015895.4:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	NP_056979.1:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAAT...
XM_005249159.1:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	XP_005249216.1:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAA...
XM_005249159.2:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	XP_005249216.1:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAA...
XM_011514651.2:c.-2321_-2320insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	XP_011512953.1:n.-2321_-2320insAGGAAAAAATTTAACATAAATAGTGTAAAA...
NM_015895.5:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA MANE Select	NP_056979.1:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAAT...
NM_001251989.2:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	NP_001238918.1:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAA...
NM_001251990.2:c.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAAAATTCATGCTCTGAAAACTACAAAA	NP_001238919.1:n.51+284_51+285insAGGAAAAAATTTAACATAAATAGTGTAA...