Canonical Allele Identifier: CA2330913639
Gene: C19orf12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.29702971_29702974delinsGCCC , CM000681.2:g.29702971_29702974delinsGCCC GRCh38
NC_000019.9:g.30193878_30193881delinsGCCC , CM000681.1:g.30193878_30193881delinsGCCC GRCh37
NC_000019.8:g.34885718_34885721delinsGCCC NCBI36
NG_031970.1:g.17816_17819delinsGGGC
NG_031970.2:g.17816_17819delinsGGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000614091.5:c.164_167delinsGGGC ENSP00000482097.2:p.Gly55=
ENST00000623113.3:c.164_167delinsGGGC ENSP00000485413.2:p.Gly55=
ENST00000323670.14:c.164_167delinsGGGC MANE Select ENSP00000313332.9:p.Gly55=
ENST00000323670.13:c.164_167delinsGGGC ENSP00000313332.8:p.Gly55=
ENST00000342680.5:c.*78_*81delinsGGGC ENSP00000345497.5:n.*78_*81delinsGGGC
ENST00000392275.1:n.555_558delinsGGGC
ENST00000392276.1:c.-29_-26delinsGGGC ENSP00000376102.1:n.-29_-26delinsGGGC
ENST00000392278.2:c.197_200delinsGGGC ENSP00000376103.2:p.Gly66=
ENST00000591243.1:c.164_167delinsGGGC ENSP00000467516.1:p.Gly55=
ENST00000592153.5:c.164_167delinsGGGC ENSP00000467117.1:p.Gly55=
ENST00000614091.4:c.164_167delinsGGGC ENSP00000482097.1:p.Gly55=
ENST00000623113.1:c.-29_-26delinsGGGC ENSP00000485413.1:n.-29_-26delinsGGGC
NM_001031726.3:c.197_200delinsGGGC NP_001026896.2:p.Gly66=
NM_001256046.1:c.164_167delinsGGGC NP_001242975.1:p.Gly55=
NM_001256047.1:c.164_167delinsGGGC NP_001242976.1:p.Gly55=
NM_001282929.1:c.-29_-26delinsGGGC NP_001269858.1:n.-29_-26delinsGGGC
NM_001282930.1:c.-29_-26delinsGGGC NP_001269859.1:n.-29_-26delinsGGGC
NM_001282931.1:c.-29_-26delinsGGGC NP_001269860.1:n.-29_-26delinsGGGC
NM_031448.4:c.164_167delinsGGGC NP_113636.2:p.Gly55=
XM_024451734.1:c.326_329delinsGGGC XP_024307502.1:p.Gly109=
XM_024451735.1:c.164_167delinsGGGC XP_024307503.1:p.Gly55=
XM_024451736.1:c.164_167delinsGGGC XP_024307504.1:p.Gly55=
XM_024451737.1:c.164_167delinsGGGC XP_024307505.1:p.Gly55=
XM_024451738.1:c.164_167delinsGGGC XP_024307506.1:p.Gly55=
NM_001256046.2:c.164_167delinsGGGC NP_001242975.1:p.Gly55=
NM_001282930.2:c.-29_-26delinsGGGC NP_001269859.1:n.-29_-26delinsGGGC
NM_001282931.2:c.-29_-26delinsGGGC NP_001269860.1:n.-29_-26delinsGGGC
NM_031448.6:c.164_167delinsGGGC MANE Select NP_113636.2:p.Gly55=
NM_001031726.4:c.164_167delinsGGGC NP_001026896.3:p.Gly55=
NM_001256046.3:c.164_167delinsGGGC NP_001242975.1:p.Gly55=
NM_001256047.2:c.164_167delinsGGGC NP_001242976.1:p.Gly55=
NM_001282930.3:c.-29_-26delinsGGGC NP_001269859.1:n.-29_-26delinsGGGC
NM_001282931.3:c.-29_-26delinsGGGC NP_001269860.1:n.-29_-26delinsGGGC