Canonical Allele Identifier: CA2814087748

Gene: C19orf12

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29703061_29703062insAACCAAACACACCCAAC , CM000681.2:g.29703061_29703062insAACCAAACACACCCAAC	GRCh38
NC_000019.9:g.30193968_30193969insAACCAAACACACCCAAC , CM000681.1:g.30193968_30193969insAACCAAACACACCCAAC	GRCh37
NC_000019.8:g.34885808_34885809insAACCAAACACACCCAAC	NCBI36
NG_031970.1:g.17728_17729insGTTGGGTGTGTTTGGTT
NG_031970.2:g.17728_17729insGTTGGGTGTGTTTGGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614091.5:c.161-85_161-84insGTTGGGTGTGTTTGGTT	ENSP00000482097.2:n.161-85_161-84insGTTGGGTGTGTTTGGTT
ENST00000623113.3:c.161-85_161-84insGTTGGGTGTGTTTGGTT	ENSP00000485413.2:n.161-85_161-84insGTTGGGTGTGTTTGGTT
ENST00000323670.14:c.161-85_161-84insGTTGGGTGTGTTTGGTT MANE Select	ENSP00000313332.9:n.161-85_161-84insGTTGGGTGTGTTTGGTT
ENST00000323670.13:c.161-85_161-84insGTTGGGTGTGTTTGGTT	ENSP00000313332.8:n.161-85_161-84insGTTGGGTGTGTTTGGTT
ENST00000342680.5:c.*75-85_*75-84insGTTGGGTGTGTTTGGTT	ENSP00000345497.5:n.*75-85_*75-84insGTTGGGTGTGTTTGGTT
ENST00000392275.1:n.552-85_552-84insGTTGGGTGTGTTTGGTT
ENST00000392276.1:c.-32-85_-32-84insGTTGGGTGTGTTTGGTT	ENSP00000376102.1:n.-32-85_-32-84insGTTGGGTGTGTTTGGTT
ENST00000392278.2:c.194-85_194-84insGTTGGGTGTGTTTGGTT	ENSP00000376103.2:n.194-85_194-84insGTTGGGTGTGTTTGGTT
ENST00000591243.1:c.161-85_161-84insGTTGGGTGTGTTTGGTT	ENSP00000467516.1:n.161-85_161-84insGTTGGGTGTGTTTGGTT
ENST00000592153.5:c.161-85_161-84insGTTGGGTGTGTTTGGTT	ENSP00000467117.1:n.161-85_161-84insGTTGGGTGTGTTTGGTT
ENST00000614091.4:c.161-85_161-84insGTTGGGTGTGTTTGGTT	ENSP00000482097.1:n.161-85_161-84insGTTGGGTGTGTTTGGTT
ENST00000623113.1:c.-32-85_-32-84insGTTGGGTGTGTTTGGTT	ENSP00000485413.1:n.-32-85_-32-84insGTTGGGTGTGTTTGGTT
NM_001031726.3:c.194-85_194-84insGTTGGGTGTGTTTGGTT	NP_001026896.2:n.194-85_194-84insGTTGGGTGTGTTTGGTT
NM_001256046.1:c.161-85_161-84insGTTGGGTGTGTTTGGTT	NP_001242975.1:n.161-85_161-84insGTTGGGTGTGTTTGGTT
NM_001256047.1:c.161-85_161-84insGTTGGGTGTGTTTGGTT	NP_001242976.1:n.161-85_161-84insGTTGGGTGTGTTTGGTT
NM_001282929.1:c.-32-85_-32-84insGTTGGGTGTGTTTGGTT	NP_001269858.1:n.-32-85_-32-84insGTTGGGTGTGTTTGGTT
NM_001282930.1:c.-32-85_-32-84insGTTGGGTGTGTTTGGTT	NP_001269859.1:n.-32-85_-32-84insGTTGGGTGTGTTTGGTT
NM_001282931.1:c.-32-85_-32-84insGTTGGGTGTGTTTGGTT	NP_001269860.1:n.-32-85_-32-84insGTTGGGTGTGTTTGGTT
NM_031448.4:c.161-85_161-84insGTTGGGTGTGTTTGGTT	NP_113636.2:n.161-85_161-84insGTTGGGTGTGTTTGGTT
XM_024451734.1:c.323-85_323-84insGTTGGGTGTGTTTGGTT	XP_024307502.1:n.323-85_323-84insGTTGGGTGTGTTTGGTT
XM_024451735.1:c.161-85_161-84insGTTGGGTGTGTTTGGTT	XP_024307503.1:n.161-85_161-84insGTTGGGTGTGTTTGGTT
XM_024451736.1:c.161-85_161-84insGTTGGGTGTGTTTGGTT	XP_024307504.1:n.161-85_161-84insGTTGGGTGTGTTTGGTT
XM_024451737.1:c.161-85_161-84insGTTGGGTGTGTTTGGTT	XP_024307505.1:n.161-85_161-84insGTTGGGTGTGTTTGGTT
XM_024451738.1:c.161-85_161-84insGTTGGGTGTGTTTGGTT	XP_024307506.1:n.161-85_161-84insGTTGGGTGTGTTTGGTT
NM_001256046.2:c.161-85_161-84insGTTGGGTGTGTTTGGTT	NP_001242975.1:n.161-85_161-84insGTTGGGTGTGTTTGGTT
NM_001282930.2:c.-32-85_-32-84insGTTGGGTGTGTTTGGTT	NP_001269859.1:n.-32-85_-32-84insGTTGGGTGTGTTTGGTT
NM_001282931.2:c.-32-85_-32-84insGTTGGGTGTGTTTGGTT	NP_001269860.1:n.-32-85_-32-84insGTTGGGTGTGTTTGGTT
NM_031448.6:c.161-85_161-84insGTTGGGTGTGTTTGGTT MANE Select	NP_113636.2:n.161-85_161-84insGTTGGGTGTGTTTGGTT
NM_001031726.4:c.161-85_161-84insGTTGGGTGTGTTTGGTT	NP_001026896.3:n.161-85_161-84insGTTGGGTGTGTTTGGTT
NM_001256046.3:c.161-85_161-84insGTTGGGTGTGTTTGGTT	NP_001242975.1:n.161-85_161-84insGTTGGGTGTGTTTGGTT
NM_001256047.2:c.161-85_161-84insGTTGGGTGTGTTTGGTT	NP_001242976.1:n.161-85_161-84insGTTGGGTGTGTTTGGTT
NM_001282930.3:c.-32-85_-32-84insGTTGGGTGTGTTTGGTT	NP_001269859.1:n.-32-85_-32-84insGTTGGGTGTGTTTGGTT
NM_001282931.3:c.-32-85_-32-84insGTTGGGTGTGTTTGGTT	NP_001269860.1:n.-32-85_-32-84insGTTGGGTGTGTTTGGTT