Canonical Allele Identifier: CA2390633816

Gene: UMODL1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42082652C>G , CM000683.2:g.42082652C>G	GRCh38
NC_000021.8:g.43502762C>G , CM000683.1:g.43502762C>G	GRCh37
NC_000021.7:g.42375831C>G	NCBI36
NG_055246.1:g.24694C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000408910.7:c.320-1432C>G MANE Select	ENSP00000386147.2:n.320-1432C>G
ENST00000400424.6:c.104-1432C>G	ENSP00000383276.1:n.104-1432C>G
ENST00000400427.5:c.104-1432C>G	ENSP00000383279.1:n.104-1432C>G
ENST00000408910.6:c.320-1432C>G	ENSP00000386147.2:n.320-1432C>G
ENST00000408989.6:c.320-1432C>G	ENSP00000386126.2:n.320-1432C>G
NM_001004416.2:c.320-1432C>G	NP_001004416.2:n.320-1432C>G
NM_001199527.1:c.104-1432C>G	NP_001186456.1:n.104-1432C>G
NM_001199528.2:c.104-1432C>G	NP_001186457.2:n.104-1432C>G
NM_173568.3:c.320-1432C>G	NP_775839.3:n.320-1432C>G
XM_011529787.1:c.104-1432C>G	XP_011528089.1:n.104-1432C>G
XM_011529788.1:c.104-1432C>G	XP_011528090.1:n.104-1432C>G
XM_011529789.1:c.104-1432C>G	XP_011528091.1:n.104-1432C>G
XM_011529790.1:c.7+611C>G	XP_011528092.1:n.7+611C>G
XM_011529791.1:c.7+611C>G	XP_011528093.1:n.7+611C>G
XM_011529793.1:c.7+611C>G	XP_011528095.1:n.7+611C>G
XM_011529794.1:c.7+611C>G	XP_011528096.1:n.7+611C>G
XM_011529795.1:c.7+611C>G	XP_011528097.1:n.7+611C>G
XM_011529796.1:c.104-1432C>G	XP_011528098.1:n.104-1432C>G
XM_011529799.1:c.104-1432C>G	XP_011528101.1:n.104-1432C>G
XM_011529803.1:c.104-1432C>G	XP_011528105.1:n.104-1432C>G
XR_937578.1:n.174-1432C>G
XR_937579.1:n.174-1432C>G
XR_937580.1:n.174-1432C>G
XM_017028506.1:c.104-1432C>G	XP_016883995.1:n.104-1432C>G
XM_017028507.1:c.7+611C>G	XP_016883996.1:n.7+611C>G
NM_001199527.2:c.104-1432C>G	NP_001186456.2:n.104-1432C>G
NM_001199528.3:c.104-1432C>G	NP_001186457.3:n.104-1432C>G
NM_001004416.3:c.320-1432C>G MANE Select	NP_001004416.3:n.320-1432C>G
NM_001199527.3:c.104-1432C>G	NP_001186456.2:n.104-1432C>G
NM_001199528.4:c.104-1432C>G	NP_001186457.3:n.104-1432C>G
NM_173568.4:c.320-1432C>G	NP_775839.4:n.320-1432C>G