Canonical Allele Identifier: CA405142823

Gene: C19orf12

Linked Data

• MyVariant Identifiers: chr19:g.30193740G>C (hg19) ; chr19:g.29702833G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29702833G>C , CM000681.2:g.29702833G>C	GRCh38
NC_000019.9:g.30193740G>C , CM000681.1:g.30193740G>C	GRCh37
NC_000019.8:g.34885580G>C	NCBI36
NG_031970.1:g.17957C>G
NG_031970.2:g.17957C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000614091.5:c.305C>G	ENSP00000482097.2:p.Thr102Arg
ENST00000623113.3:c.305C>G	ENSP00000485413.2:p.Thr102Arg
ENST00000323670.14:c.305C>G MANE Select	ENSP00000313332.9:p.Thr102Arg
ENST00000323670.13:c.305C>G	ENSP00000313332.8:p.Thr102Arg
ENST00000392275.1:n.696C>G
ENST00000392276.1:c.113C>G	ENSP00000376102.1:p.Thr38Arg
ENST00000392278.2:c.338C>G	ENSP00000376103.2:p.Thr113Arg
ENST00000591243.1:c.305C>G	ENSP00000467516.1:p.Thr102Arg
ENST00000592153.5:c.290+15C>G	ENSP00000467117.1:n.290+15C>G
ENST00000614091.4:c.305C>G	ENSP00000482097.1:p.Thr102Arg
ENST00000623113.1:c.113C>G	ENSP00000485413.1:p.Thr38Arg
NM_001031726.3:c.338C>G	NP_001026896.2:p.Thr113Arg
NM_001256046.1:c.290+15C>G	NP_001242975.1:n.290+15C>G
NM_001256047.1:c.305C>G	NP_001242976.1:p.Thr102Arg
NM_001282929.1:c.113C>G	NP_001269858.1:p.Thr38Arg
NM_001282930.1:c.113C>G	NP_001269859.1:p.Thr38Arg
NM_001282931.1:c.113C>G	NP_001269860.1:p.Thr38Arg
NM_031448.4:c.305C>G	NP_113636.2:p.Thr102Arg
XM_024451734.1:c.467C>G	XP_024307502.1:p.Thr156Arg
XM_024451735.1:c.305C>G	XP_024307503.1:p.Thr102Arg
XM_024451736.1:c.305C>G	XP_024307504.1:p.Thr102Arg
XM_024451737.1:c.305C>G	XP_024307505.1:p.Thr102Arg
XM_024451738.1:c.305C>G	XP_024307506.1:p.Thr102Arg
NM_001256046.2:c.290+15C>G	NP_001242975.1:n.290+15C>G
NM_001282930.2:c.113C>G	NP_001269859.1:p.Thr38Arg
NM_001282931.2:c.113C>G	NP_001269860.1:p.Thr38Arg
NM_031448.6:c.305C>G MANE Select	NP_113636.2:p.Thr102Arg
NM_001031726.4:c.305C>G	NP_001026896.3:p.Thr102Arg
NM_001256046.3:c.290+15C>G	NP_001242975.1:n.290+15C>G
NM_001256047.2:c.305C>G	NP_001242976.1:p.Thr102Arg
NM_001282930.3:c.113C>G	NP_001269859.1:p.Thr38Arg
NM_001282931.3:c.113C>G	NP_001269860.1:p.Thr38Arg