Canonical Allele Identifier: CA10651734

Gene: C19orf12

Linked Data

• ClinVar Variation Id: 328732
• ClinVar RCV Id: RCV000270466
• dbSNP Id: rs886054323
• MyVariant Identifiers: chr19:g.30199342A>T (hg19) ; chr19:g.29708435A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29708435A>T , CM000681.2:g.29708435A>T	GRCh38
NC_000019.9:g.30199342A>T , CM000681.1:g.30199342A>T	GRCh37
NC_000019.8:g.34891182A>T	NCBI36
NG_031970.1:g.12355T>A
NG_031970.2:g.12355T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614091.5:c.-10-12T>A	ENSP00000482097.2:n.-10-12T>A
ENST00000623113.3:c.-10-12T>A	ENSP00000485413.2:n.-10-12T>A
ENST00000323670.14:c.-10-12T>A MANE Select	ENSP00000313332.9:n.-10-12T>A
ENST00000323670.13:c.-10-12T>A	ENSP00000313332.8:n.-10-12T>A
ENST00000342680.5:c.-10-12T>A	ENSP00000345497.5:n.-10-12T>A
ENST00000392275.1:n.552-5458T>A
ENST00000392276.1:c.-32-5458T>A	ENSP00000376102.1:n.-32-5458T>A
ENST00000392278.2:c.24-12T>A	ENSP00000376103.2:n.24-12T>A
ENST00000591243.1:c.-22T>A	ENSP00000467516.1:n.-22T>A
ENST00000592153.5:c.-10-12T>A	ENSP00000467117.1:n.-10-12T>A
ENST00000614091.4:c.-10-12T>A	ENSP00000482097.1:n.-10-12T>A
ENST00000623113.1:c.-32-5458T>A	ENSP00000485413.1:n.-32-5458T>A
NM_001031726.3:c.24-12T>A	NP_001026896.2:n.24-12T>A
NM_001256046.1:c.-10-12T>A	NP_001242975.1:n.-10-12T>A
NM_001256047.1:c.-10-12T>A	NP_001242976.1:n.-10-12T>A
NM_001282929.1:c.-32-5458T>A	NP_001269858.1:n.-32-5458T>A
NM_001282930.1:c.-32-5458T>A	NP_001269859.1:n.-32-5458T>A
NM_001282931.1:c.-323-12T>A	NP_001269860.1:n.-323-12T>A
NM_031448.4:c.-10-12T>A	NP_113636.2:n.-10-12T>A
XM_024451734.1:c.153-12T>A	XP_024307502.1:n.153-12T>A
XM_024451735.1:c.-10-12T>A	XP_024307503.1:n.-10-12T>A
XM_024451736.1:c.-10-12T>A	XP_024307504.1:n.-10-12T>A
XM_024451737.1:c.-10-12T>A	XP_024307505.1:n.-10-12T>A
XM_024451738.1:c.-10-12T>A	XP_024307506.1:n.-10-12T>A
NM_001256046.2:c.-10-12T>A	NP_001242975.1:n.-10-12T>A
NM_001282930.2:c.-32-5458T>A	NP_001269859.1:n.-32-5458T>A
NM_001282931.2:c.-323-12T>A	NP_001269860.1:n.-323-12T>A
NM_031448.6:c.-10-12T>A MANE Select	NP_113636.2:n.-10-12T>A
NM_001031726.4:c.-10-12T>A	NP_001026896.3:n.-10-12T>A
NM_001256046.3:c.-10-12T>A	NP_001242975.1:n.-10-12T>A
NM_001256047.2:c.-10-12T>A	NP_001242976.1:n.-10-12T>A
NM_001282930.3:c.-32-5458T>A	NP_001269859.1:n.-32-5458T>A
NM_001282931.3:c.-323-12T>A	NP_001269860.1:n.-323-12T>A