Canonical Allele Identifier: CA506988081

Gene: C19orf12

Linked Data

• MyVariant Identifiers: chr19:g.30193816G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29702909G>A , CM000681.2:g.29702909G>A	GRCh38
NC_000019.9:g.30193816G>A , CM000681.1:g.30193816G>A	GRCh37
NC_000019.8:g.34885656G>A	NCBI36
NG_031970.1:g.17881C>T
NG_031970.2:g.17881C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614091.5:c.229C>T	ENSP00000482097.2:p.Leu77=
ENST00000623113.3:c.229C>T	ENSP00000485413.2:p.Leu77=
ENST00000323670.14:c.229C>T MANE Select	ENSP00000313332.9:p.Leu77=
ENST00000323670.13:c.229C>T	ENSP00000313332.8:p.Leu77=
ENST00000342680.5:c.*143C>T	ENSP00000345497.5:n.*143C>T
ENST00000392275.1:n.620C>T
ENST00000392276.1:c.37C>T	ENSP00000376102.1:p.Leu13=
ENST00000392278.2:c.262C>T	ENSP00000376103.2:p.Leu88=
ENST00000591243.1:c.229C>T	ENSP00000467516.1:p.Leu77=
ENST00000592153.5:c.229C>T	ENSP00000467117.1:p.Leu77=
ENST00000614091.4:c.229C>T	ENSP00000482097.1:p.Leu77=
ENST00000623113.1:c.37C>T	ENSP00000485413.1:p.Leu13=
NM_001031726.3:c.262C>T	NP_001026896.2:p.Leu88=
NM_001256046.1:c.229C>T	NP_001242975.1:p.Leu77=
NM_001256047.1:c.229C>T	NP_001242976.1:p.Leu77=
NM_001282929.1:c.37C>T	NP_001269858.1:p.Leu13=
NM_001282930.1:c.37C>T	NP_001269859.1:p.Leu13=
NM_001282931.1:c.37C>T	NP_001269860.1:p.Leu13=
NM_031448.4:c.229C>T	NP_113636.2:p.Leu77=
XM_024451734.1:c.391C>T	XP_024307502.1:p.Leu131=
XM_024451735.1:c.229C>T	XP_024307503.1:p.Leu77=
XM_024451736.1:c.229C>T	XP_024307504.1:p.Leu77=
XM_024451737.1:c.229C>T	XP_024307505.1:p.Leu77=
XM_024451738.1:c.229C>T	XP_024307506.1:p.Leu77=
NM_001256046.2:c.229C>T	NP_001242975.1:p.Leu77=
NM_001282930.2:c.37C>T	NP_001269859.1:p.Leu13=
NM_001282931.2:c.37C>T	NP_001269860.1:p.Leu13=
NM_031448.6:c.229C>T MANE Select	NP_113636.2:p.Leu77=
NM_001031726.4:c.229C>T	NP_001026896.3:p.Leu77=
NM_001256046.3:c.229C>T	NP_001242975.1:p.Leu77=
NM_001256047.2:c.229C>T	NP_001242976.1:p.Leu77=
NM_001282930.3:c.37C>T	NP_001269859.1:p.Leu13=
NM_001282931.3:c.37C>T	NP_001269860.1:p.Leu13=