Canonical Allele Identifier: CA2838208078

Gene: MORN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2372628G>T , CM000663.2:g.2372628G>T	GRCh38
NC_000001.10:g.2304067G>T , CM000663.1:g.2304067G>T	GRCh37
NC_000001.9:g.2293927G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378531.8:c.635-37C>A MANE Select	ENSP00000367792.3:n.635-37C>A
ENST00000378529.7:c.635-37C>A	ENSP00000367790.3:n.635-37C>A
ENST00000378531.7:c.635-37C>A	ENSP00000367792.3:n.635-37C>A
ENST00000419785.1:n.242-37C>A
ENST00000469374.5:n.481-37C>A
ENST00000606372.5:n.717-37C>A
ENST00000607342.5:n.378-37C>A
NM_001301060.1:c.635-37C>A	NP_001287989.1:n.635-37C>A
NM_024848.2:c.635-37C>A	NP_079124.1:n.635-37C>A
XM_005244798.2:c.563-37C>A	XP_005244855.1:n.563-37C>A
XM_011542169.1:c.635-37C>A	XP_011540471.1:n.635-37C>A
XM_011542170.1:c.635-37C>A	XP_011540472.1:n.635-37C>A
XM_011542171.1:c.584-37C>A	XP_011540473.1:n.584-37C>A
XM_011542172.1:c.563-37C>A	XP_011540474.1:n.563-37C>A
XM_011542173.1:c.635-37C>A	XP_011540475.1:n.635-37C>A
XM_011542174.1:c.635-37C>A	XP_011540476.1:n.635-37C>A
XM_011542175.1:c.635-37C>A	XP_011540477.1:n.635-37C>A
XM_011542176.1:c.635-37C>A	XP_011540478.1:n.635-37C>A
XM_011542177.1:c.635-37C>A	XP_011540479.1:n.635-37C>A
XR_946762.1:n.853-37C>A
XM_005244798.3:c.563-37C>A	XP_005244855.1:n.563-37C>A
XM_011542169.2:c.635-37C>A	XP_011540471.1:n.635-37C>A
XM_011542170.2:c.635-37C>A	XP_011540472.1:n.635-37C>A
XM_011542172.2:c.563-37C>A	XP_011540474.1:n.563-37C>A
XM_011542173.2:c.635-37C>A	XP_011540475.1:n.635-37C>A
XM_011542174.2:c.635-37C>A	XP_011540476.1:n.635-37C>A
XM_011542176.2:c.635-37C>A	XP_011540478.1:n.635-37C>A
XM_017002365.1:c.635-37C>A	XP_016857854.1:n.635-37C>A
XM_024449843.1:c.635-37C>A	XP_024305611.1:n.635-37C>A
NM_024848.3:c.635-37C>A MANE Select	NP_079124.1:n.635-37C>A
NM_001301060.2:c.635-37C>A	NP_001287989.1:n.635-37C>A