Canonical Allele Identifier: CA2814087727

Gene: C19orf12

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29702946_29702947insGTGCCTGGATGA , CM000681.2:g.29702946_29702947insGTGCCTGGATGA	GRCh38
NC_000019.9:g.30193853_30193854insGTGCCTGGATGA , CM000681.1:g.30193853_30193854insGTGCCTGGATGA	GRCh37
NC_000019.8:g.34885693_34885694insGTGCCTGGATGA	NCBI36
NG_031970.1:g.17843_17844insTCATCCAGGCAC
NG_031970.2:g.17843_17844insTCATCCAGGCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614091.5:c.191_192insTCATCCAGGCAC	ENSP00000482097.2:p.Trp64delinsCysHisProGlyThr
ENST00000623113.3:c.191_192insTCATCCAGGCAC	ENSP00000485413.2:p.Trp64delinsCysHisProGlyThr
ENST00000323670.14:c.191_192insTCATCCAGGCAC MANE Select	ENSP00000313332.9:p.Trp64delinsCysHisProGlyThr
ENST00000323670.13:c.191_192insTCATCCAGGCAC	ENSP00000313332.8:p.Trp64delinsCysHisProGlyThr
ENST00000342680.5:c.*105_*106insTCATCCAGGCAC	ENSP00000345497.5:n.*105_*106insTCATCCAGGCAC
ENST00000392275.1:n.582_583insTCATCCAGGCAC
ENST00000392276.1:c.-2_-1insTCATCCAGGCAC	ENSP00000376102.1:n.-2_-1insTCATCCAGGCAC
ENST00000392278.2:c.224_225insTCATCCAGGCAC	ENSP00000376103.2:p.Trp75delinsCysHisProGlyThr
ENST00000591243.1:c.191_192insTCATCCAGGCAC	ENSP00000467516.1:p.Trp64delinsCysHisProGlyThr
ENST00000592153.5:c.191_192insTCATCCAGGCAC	ENSP00000467117.1:p.Trp64delinsCysHisProGlyThr
ENST00000614091.4:c.191_192insTCATCCAGGCAC	ENSP00000482097.1:p.Trp64delinsCysHisProGlyThr
ENST00000623113.1:c.-2_-1insTCATCCAGGCAC	ENSP00000485413.1:n.-2_-1insTCATCCAGGCAC
NM_001031726.3:c.224_225insTCATCCAGGCAC	NP_001026896.2:p.Trp75delinsCysHisProGlyThr
NM_001256046.1:c.191_192insTCATCCAGGCAC	NP_001242975.1:p.Trp64delinsCysHisProGlyThr
NM_001256047.1:c.191_192insTCATCCAGGCAC	NP_001242976.1:p.Trp64delinsCysHisProGlyThr
NM_001282929.1:c.-2_-1insTCATCCAGGCAC	NP_001269858.1:n.-2_-1insTCATCCAGGCAC
NM_001282930.1:c.-2_-1insTCATCCAGGCAC	NP_001269859.1:n.-2_-1insTCATCCAGGCAC
NM_001282931.1:c.-2_-1insTCATCCAGGCAC	NP_001269860.1:n.-2_-1insTCATCCAGGCAC
NM_031448.4:c.191_192insTCATCCAGGCAC	NP_113636.2:p.Trp64delinsCysHisProGlyThr
XM_024451734.1:c.353_354insTCATCCAGGCAC	XP_024307502.1:p.Trp118delinsCysHisProGlyThr
XM_024451735.1:c.191_192insTCATCCAGGCAC	XP_024307503.1:p.Trp64delinsCysHisProGlyThr
XM_024451736.1:c.191_192insTCATCCAGGCAC	XP_024307504.1:p.Trp64delinsCysHisProGlyThr
XM_024451737.1:c.191_192insTCATCCAGGCAC	XP_024307505.1:p.Trp64delinsCysHisProGlyThr
XM_024451738.1:c.191_192insTCATCCAGGCAC	XP_024307506.1:p.Trp64delinsCysHisProGlyThr
NM_001256046.2:c.191_192insTCATCCAGGCAC	NP_001242975.1:p.Trp64delinsCysHisProGlyThr
NM_001282930.2:c.-2_-1insTCATCCAGGCAC	NP_001269859.1:n.-2_-1insTCATCCAGGCAC
NM_001282931.2:c.-2_-1insTCATCCAGGCAC	NP_001269860.1:n.-2_-1insTCATCCAGGCAC
NM_031448.6:c.191_192insTCATCCAGGCAC MANE Select	NP_113636.2:p.Trp64delinsCysHisProGlyThr
NM_001031726.4:c.191_192insTCATCCAGGCAC	NP_001026896.3:p.Trp64delinsCysHisProGlyThr
NM_001256046.3:c.191_192insTCATCCAGGCAC	NP_001242975.1:p.Trp64delinsCysHisProGlyThr
NM_001256047.2:c.191_192insTCATCCAGGCAC	NP_001242976.1:p.Trp64delinsCysHisProGlyThr
NM_001282930.3:c.-2_-1insTCATCCAGGCAC	NP_001269859.1:n.-2_-1insTCATCCAGGCAC
NM_001282931.3:c.-2_-1insTCATCCAGGCAC	NP_001269860.1:n.-2_-1insTCATCCAGGCAC