Canonical Allele Identifier: CA2330913544
Gene: C19orf12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.29702801C= , CM000681.2:g.29702801C= GRCh38
NC_000019.9:g.30193708C= , CM000681.1:g.30193708C= GRCh37
NC_000019.8:g.34885548C= NCBI36
NG_031970.1:g.17989G=
NG_031970.2:g.17989G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614091.5:c.337G= ENSP00000482097.2:p.Gly113=
ENST00000623113.3:c.337G= ENSP00000485413.2:p.Gly113=
ENST00000323670.14:c.337G= MANE Select ENSP00000313332.9:p.Gly113=
ENST00000323670.13:c.337G= ENSP00000313332.8:p.Gly113=
ENST00000392275.1:n.728G=
ENST00000392276.1:c.145G= ENSP00000376102.1:p.Gly49=
ENST00000392278.2:c.370G= ENSP00000376103.2:p.Gly124=
ENST00000592153.5:c.291-9G= ENSP00000467117.1:n.291-9G=
ENST00000614091.4:c.337G= ENSP00000482097.1:p.Gly113=
ENST00000623113.1:c.145G= ENSP00000485413.1:p.Gly49=
NM_001031726.3:c.370G= NP_001026896.2:p.Gly124=
NM_001256046.1:c.291-9G= NP_001242975.1:n.291-9G=
NM_001256047.1:c.337G= NP_001242976.1:p.Gly113=
NM_001282929.1:c.145G= NP_001269858.1:p.Gly49=
NM_001282930.1:c.145G= NP_001269859.1:p.Gly49=
NM_001282931.1:c.145G= NP_001269860.1:p.Gly49=
NM_031448.4:c.337G= NP_113636.2:p.Gly113=
XM_024451734.1:c.499G= XP_024307502.1:p.Gly167=
XM_024451735.1:c.337G= XP_024307503.1:p.Gly113=
XM_024451736.1:c.337G= XP_024307504.1:p.Gly113=
XM_024451737.1:c.337G= XP_024307505.1:p.Gly113=
XM_024451738.1:c.337G= XP_024307506.1:p.Gly113=
NM_001256046.2:c.291-9G= NP_001242975.1:n.291-9G=
NM_001282930.2:c.145G= NP_001269859.1:p.Gly49=
NM_001282931.2:c.145G= NP_001269860.1:p.Gly49=
NM_031448.6:c.337G= MANE Select NP_113636.2:p.Gly113=
NM_001031726.4:c.337G= NP_001026896.3:p.Gly113=
NM_001256046.3:c.291-9G= NP_001242975.1:n.291-9G=
NM_001256047.2:c.337G= NP_001242976.1:p.Gly113=
NM_001282930.3:c.145G= NP_001269859.1:p.Gly49=
NM_001282931.3:c.145G= NP_001269860.1:p.Gly49=