Canonical Allele Identifier: CA405142691

Gene: C19orf12

Linked Data

• ClinVar Variation Id: 1251967
• ClinVar RCV Id: RCV001644555
• dbSNP Id: rs1972173461
• MyVariant Identifiers: chr19:g.30193713A>G (hg19) ; chr19:g.29702806A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29702806A>G , CM000681.2:g.29702806A>G	GRCh38
NC_000019.9:g.30193713A>G , CM000681.1:g.30193713A>G	GRCh37
NC_000019.8:g.34885553A>G	NCBI36
NG_031970.1:g.17984T>C
NG_031970.2:g.17984T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614091.5:c.332T>C	ENSP00000482097.2:p.Val111Ala
ENST00000623113.3:c.332T>C	ENSP00000485413.2:p.Val111Ala
ENST00000323670.14:c.332T>C MANE Select	ENSP00000313332.9:p.Val111Ala
ENST00000323670.13:c.332T>C	ENSP00000313332.8:p.Val111Ala
ENST00000392275.1:n.723T>C
ENST00000392276.1:c.140T>C	ENSP00000376102.1:p.Val47Ala
ENST00000392278.2:c.365T>C	ENSP00000376103.2:p.Val122Ala
ENST00000592153.5:c.291-14T>C	ENSP00000467117.1:n.291-14T>C
ENST00000614091.4:c.332T>C	ENSP00000482097.1:p.Val111Ala
ENST00000623113.1:c.140T>C	ENSP00000485413.1:p.Val47Ala
NM_001031726.3:c.365T>C	NP_001026896.2:p.Val122Ala
NM_001256046.1:c.291-14T>C	NP_001242975.1:n.291-14T>C
NM_001256047.1:c.332T>C	NP_001242976.1:p.Val111Ala
NM_001282929.1:c.140T>C	NP_001269858.1:p.Val47Ala
NM_001282930.1:c.140T>C	NP_001269859.1:p.Val47Ala
NM_001282931.1:c.140T>C	NP_001269860.1:p.Val47Ala
NM_031448.4:c.332T>C	NP_113636.2:p.Val111Ala
XM_024451734.1:c.494T>C	XP_024307502.1:p.Val165Ala
XM_024451735.1:c.332T>C	XP_024307503.1:p.Val111Ala
XM_024451736.1:c.332T>C	XP_024307504.1:p.Val111Ala
XM_024451737.1:c.332T>C	XP_024307505.1:p.Val111Ala
XM_024451738.1:c.332T>C	XP_024307506.1:p.Val111Ala
NM_001256046.2:c.291-14T>C	NP_001242975.1:n.291-14T>C
NM_001282930.2:c.140T>C	NP_001269859.1:p.Val47Ala
NM_001282931.2:c.140T>C	NP_001269860.1:p.Val47Ala
NM_031448.6:c.332T>C MANE Select	NP_113636.2:p.Val111Ala
NM_001031726.4:c.332T>C	NP_001026896.3:p.Val111Ala
NM_001256046.3:c.291-14T>C	NP_001242975.1:n.291-14T>C
NM_001256047.2:c.332T>C	NP_001242976.1:p.Val111Ala
NM_001282930.3:c.140T>C	NP_001269859.1:p.Val47Ala
NM_001282931.3:c.140T>C	NP_001269860.1:p.Val47Ala