Canonical Allele Identifier: CA621658528

Gene: UMOD

Linked Data

• dbSNP Id: rs1469263285
• gnomAD v2: 16-20359735-A-AATGTATGTGAAGTATTGAAAACAGCGC
• MyVariant Identifiers: chr16:g.20359735_20359736insATGTATGTGAAGTATTGAAAACAGCGC (hg19) ; chr16:g.20348413_20348414insATGTATGTGAAGTATTGAAAACAGCGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20348413_20348414insATGTATGTGAAGTATTGAAAACAGCGC , CM000678.2:g.20348413_20348414insATGTATGTGAAGTATTGAAAACAGCGC	GRCh38
NC_000016.9:g.20359735_20359736insATGTATGTGAAGTATTGAAAACAGCGC , CM000678.1:g.20359735_20359736insATGTATGTGAAGTATTGAAAACAGCGC	GRCh37
NC_000016.8:g.20267236_20267237insATGTATGTGAAGTATTGAAAACAGCGC	NCBI36
NG_008151.1:g.9302_9303insGCGCTGTTTTCAATACTTCACATACAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396138.9:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT MANE Select	ENSP00000379442.5:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATAC...
ENST00000302509.8:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	ENSP00000306279.4:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATAC...
ENST00000396134.6:c.964+22_964+23insGCGCTGTTTTCAATACTTCACATACAT	ENSP00000379438.2:n.964+22_964+23insGCGCTGTTTTCAATACTTCACATAC...
ENST00000396138.8:c.1012+22_1012+23insGCGCTGTTTTCAATACTTCACATACAT	ENSP00000379442.4:n.1012+22_1012+23insGCGCTGTTTTCAATACTTCACAT...
ENST00000570689.5:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	ENSP00000460548.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATAC...
NM_001008389.2:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	NP_001008390.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
NM_001278614.1:c.964+22_964+23insGCGCTGTTTTCAATACTTCACATACAT	NP_001265543.1:n.964+22_964+23insGCGCTGTTTTCAATACTTCACATACAT
NM_003361.3:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	NP_003352.2:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
XM_011545934.1:c.949+22_949+23insGCGCTGTTTTCAATACTTCACATACAT	XP_011544236.1:n.949+22_949+23insGCGCTGTTTTCAATACTTCACATACAT
XM_011545935.1:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	XP_011544237.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
XM_011545936.1:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	XP_011544238.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
XM_011545937.1:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	XP_011544239.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
XM_011545938.1:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	XP_011544240.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
XM_011545939.1:c.949+22_949+23insGCGCTGTTTTCAATACTTCACATACAT	XP_011544241.1:n.949+22_949+23insGCGCTGTTTTCAATACTTCACATACAT
XM_011545940.1:c.1012+22_1012+23insGCGCTGTTTTCAATACTTCACATACAT	XP_011544242.1:n.1012+22_1012+23insGCGCTGTTTTCAATACTTCACATACA...
XM_011545934.2:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	XP_011544236.2:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
XM_011545940.2:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	XP_011544242.2:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
XM_024450433.1:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	XP_024306201.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
NM_001008389.3:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	NP_001008390.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
NM_001278614.2:c.964+22_964+23insGCGCTGTTTTCAATACTTCACATACAT	NP_001265543.1:n.964+22_964+23insGCGCTGTTTTCAATACTTCACATACAT
NM_001378232.1:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	NP_001365161.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
NM_001378233.1:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	NP_001365162.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
NM_001378234.1:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	NP_001365163.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
NM_001378235.1:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	NP_001365164.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
NM_001378237.1:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT	NP_001365166.1:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
NM_003361.4:c.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT MANE Select	NP_003352.2:n.865+22_865+23insGCGCTGTTTTCAATACTTCACATACAT
NR_165456.1:n.1090+22_1090+23insGCGCTGTTTTCAATACTTCACATACAT