Canonical Allele Identifier: CA405142567

Gene: C19orf12

Linked Data

• MyVariant Identifiers: chr19:g.30193693G>C (hg19) ; chr19:g.29702786G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29702786G>C , CM000681.2:g.29702786G>C	GRCh38
NC_000019.9:g.30193693G>C , CM000681.1:g.30193693G>C	GRCh37
NC_000019.8:g.34885533G>C	NCBI36
NG_031970.1:g.18004C>G
NG_031970.2:g.18004C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623113.3:c.352C>G	ENSP00000485413.2:p.Gln118Glu
ENST00000323670.14:c.352C>G MANE Select	ENSP00000313332.9:p.Gln118Glu
ENST00000323670.13:c.352C>G	ENSP00000313332.8:p.Gln118Glu
ENST00000392275.1:n.743C>G
ENST00000392276.1:c.160C>G	ENSP00000376102.1:p.Gln54Glu
ENST00000392278.2:c.385C>G	ENSP00000376103.2:p.Gln129Glu
ENST00000592153.5:c.297C>G	ENSP00000467117.1:p.Cys99Trp
ENST00000614091.4:c.352C>G	ENSP00000482097.1:p.Gln118Glu
ENST00000623113.1:c.160C>G	ENSP00000485413.1:p.Gln54Glu
NM_001031726.3:c.385C>G	NP_001026896.2:p.Gln129Glu
NM_001256046.1:c.297C>G	NP_001242975.1:p.Cys99Trp
NM_001256047.1:c.352C>G	NP_001242976.1:p.Gln118Glu
NM_001282929.1:c.160C>G	NP_001269858.1:p.Gln54Glu
NM_001282930.1:c.160C>G	NP_001269859.1:p.Gln54Glu
NM_001282931.1:c.160C>G	NP_001269860.1:p.Gln54Glu
NM_031448.4:c.352C>G	NP_113636.2:p.Gln118Glu
XM_024451734.1:c.514C>G	XP_024307502.1:p.Gln172Glu
XM_024451735.1:c.352C>G	XP_024307503.1:p.Gln118Glu
XM_024451736.1:c.352C>G	XP_024307504.1:p.Gln118Glu
XM_024451737.1:c.352C>G	XP_024307505.1:p.Gln118Glu
XM_024451738.1:c.352C>G	XP_024307506.1:p.Gln118Glu
NM_001256046.2:c.297C>G	NP_001242975.1:p.Cys99Trp
NM_001282930.2:c.160C>G	NP_001269859.1:p.Gln54Glu
NM_001282931.2:c.160C>G	NP_001269860.1:p.Gln54Glu
NM_031448.6:c.352C>G MANE Select	NP_113636.2:p.Gln118Glu
NM_001031726.4:c.352C>G	NP_001026896.3:p.Gln118Glu
NM_001256046.3:c.297C>G	NP_001242975.1:p.Cys99Trp
NM_001256047.2:c.352C>G	NP_001242976.1:p.Gln118Glu
NM_001282930.3:c.160C>G	NP_001269859.1:p.Gln54Glu
NM_001282931.3:c.160C>G	NP_001269860.1:p.Gln54Glu