Canonical Allele Identifier: CA2814087730

Gene: C19orf12

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29702948_29702949insAGTGGACGG , CM000681.2:g.29702948_29702949insAGTGGACGG	GRCh38
NC_000019.9:g.30193855_30193856insAGTGGACGG , CM000681.1:g.30193855_30193856insAGTGGACGG	GRCh37
NC_000019.8:g.34885695_34885696insAGTGGACGG	NCBI36
NG_031970.1:g.17841_17842insCCGTCCACT
NG_031970.2:g.17841_17842insCCGTCCACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614091.5:c.189_190insCCGTCCACT	ENSP00000482097.2:p.Ala63_Trp64insProSerThr
ENST00000623113.3:c.189_190insCCGTCCACT	ENSP00000485413.2:p.Ala63_Trp64insProSerThr
ENST00000323670.14:c.189_190insCCGTCCACT MANE Select	ENSP00000313332.9:p.Ala63_Trp64insProSerThr
ENST00000323670.13:c.189_190insCCGTCCACT	ENSP00000313332.8:p.Ala63_Trp64insProSerThr
ENST00000342680.5:c.*103_*104insCCGTCCACT	ENSP00000345497.5:n.*103_*104insCCGTCCACT
ENST00000392275.1:n.580_581insCCGTCCACT
ENST00000392276.1:c.-4_-3insCCGTCCACT	ENSP00000376102.1:n.-4_-3insCCGTCCACT
ENST00000392278.2:c.222_223insCCGTCCACT	ENSP00000376103.2:p.Ala74_Trp75insProSerThr
ENST00000591243.1:c.189_190insCCGTCCACT	ENSP00000467516.1:p.Ala63_Trp64insProSerThr
ENST00000592153.5:c.189_190insCCGTCCACT	ENSP00000467117.1:p.Ala63_Trp64insProSerThr
ENST00000614091.4:c.189_190insCCGTCCACT	ENSP00000482097.1:p.Ala63_Trp64insProSerThr
ENST00000623113.1:c.-4_-3insCCGTCCACT	ENSP00000485413.1:n.-4_-3insCCGTCCACT
NM_001031726.3:c.222_223insCCGTCCACT	NP_001026896.2:p.Ala74_Trp75insProSerThr
NM_001256046.1:c.189_190insCCGTCCACT	NP_001242975.1:p.Ala63_Trp64insProSerThr
NM_001256047.1:c.189_190insCCGTCCACT	NP_001242976.1:p.Ala63_Trp64insProSerThr
NM_001282929.1:c.-4_-3insCCGTCCACT	NP_001269858.1:n.-4_-3insCCGTCCACT
NM_001282930.1:c.-4_-3insCCGTCCACT	NP_001269859.1:n.-4_-3insCCGTCCACT
NM_001282931.1:c.-4_-3insCCGTCCACT	NP_001269860.1:n.-4_-3insCCGTCCACT
NM_031448.4:c.189_190insCCGTCCACT	NP_113636.2:p.Ala63_Trp64insProSerThr
XM_024451734.1:c.351_352insCCGTCCACT	XP_024307502.1:p.Ala117_Trp118insProSerThr
XM_024451735.1:c.189_190insCCGTCCACT	XP_024307503.1:p.Ala63_Trp64insProSerThr
XM_024451736.1:c.189_190insCCGTCCACT	XP_024307504.1:p.Ala63_Trp64insProSerThr
XM_024451737.1:c.189_190insCCGTCCACT	XP_024307505.1:p.Ala63_Trp64insProSerThr
XM_024451738.1:c.189_190insCCGTCCACT	XP_024307506.1:p.Ala63_Trp64insProSerThr
NM_001256046.2:c.189_190insCCGTCCACT	NP_001242975.1:p.Ala63_Trp64insProSerThr
NM_001282930.2:c.-4_-3insCCGTCCACT	NP_001269859.1:n.-4_-3insCCGTCCACT
NM_001282931.2:c.-4_-3insCCGTCCACT	NP_001269860.1:n.-4_-3insCCGTCCACT
NM_031448.6:c.189_190insCCGTCCACT MANE Select	NP_113636.2:p.Ala63_Trp64insProSerThr
NM_001031726.4:c.189_190insCCGTCCACT	NP_001026896.3:p.Ala63_Trp64insProSerThr
NM_001256046.3:c.189_190insCCGTCCACT	NP_001242975.1:p.Ala63_Trp64insProSerThr
NM_001256047.2:c.189_190insCCGTCCACT	NP_001242976.1:p.Ala63_Trp64insProSerThr
NM_001282930.3:c.-4_-3insCCGTCCACT	NP_001269859.1:n.-4_-3insCCGTCCACT
NM_001282931.3:c.-4_-3insCCGTCCACT	NP_001269860.1:n.-4_-3insCCGTCCACT