Canonical Allele Identifier: CA1139840060

Gene: MORN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2378754G= , CM000663.2:g.2378754G=	GRCh38
NC_000001.10:g.2310193G= , CM000663.1:g.2310193G=	GRCh37
NC_000001.9:g.2300053G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378531.8:c.538-4197C= MANE Select	ENSP00000367792.3:n.538-4197C=
ENST00000378525.2:c.*340C=	ENSP00000367786.2:n.*340C=
ENST00000378529.7:c.538-4197C=	ENSP00000367790.3:n.538-4197C=
ENST00000378531.7:c.538-4197C=	ENSP00000367792.3:n.538-4197C=
ENST00000419785.1:n.145-4197C=
ENST00000449373.2:c.863C=	ENSP00000390261.1:n.863C=
ENST00000469374.5:n.384-4197C=
ENST00000606372.5:n.620-4197C=
NM_001301060.1:c.538-4197C=	NP_001287989.1:n.538-4197C=
NM_024848.2:c.538-4197C=	NP_079124.1:n.538-4197C=
NR_125361.1:n.1029C=
XM_005244798.2:c.466-4197C=	XP_005244855.1:n.466-4197C=
XM_011542169.1:c.538-4197C=	XP_011540471.1:n.538-4197C=
XM_011542170.1:c.538-4197C=	XP_011540472.1:n.538-4197C=
XM_011542171.1:c.487-4197C=	XP_011540473.1:n.487-4197C=
XM_011542172.1:c.466-4197C=	XP_011540474.1:n.466-4197C=
XM_011542173.1:c.538-4197C=	XP_011540475.1:n.538-4197C=
XM_011542174.1:c.538-4197C=	XP_011540476.1:n.538-4197C=
XM_011542175.1:c.538-4197C=	XP_011540477.1:n.538-4197C=
XM_011542176.1:c.538-4197C=	XP_011540478.1:n.538-4197C=
XM_011542177.1:c.538-4197C=	XP_011540479.1:n.538-4197C=
XR_946762.1:n.756-4197C=
XM_005244798.3:c.466-4197C=	XP_005244855.1:n.466-4197C=
XM_011542169.2:c.538-4197C=	XP_011540471.1:n.538-4197C=
XM_011542170.2:c.538-4197C=	XP_011540472.1:n.538-4197C=
XM_011542172.2:c.466-4197C=	XP_011540474.1:n.466-4197C=
XM_011542173.2:c.538-4197C=	XP_011540475.1:n.538-4197C=
XM_011542174.2:c.538-4197C=	XP_011540476.1:n.538-4197C=
XM_011542176.2:c.538-4197C=	XP_011540478.1:n.538-4197C=
XM_017002365.1:c.538-4197C=	XP_016857854.1:n.538-4197C=
XM_024449843.1:c.538-4197C=	XP_024305611.1:n.538-4197C=
NM_024848.3:c.538-4197C= MANE Select	NP_079124.1:n.538-4197C=
NM_001301060.2:c.538-4197C=	NP_001287989.1:n.538-4197C=
NR_125361.2:n.832C=