Canonical Allele Identifier: CA2814086659

Gene: C19orf12

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29708140A>C , CM000681.2:g.29708140A>C	GRCh38
NC_000019.9:g.30199047A>C , CM000681.1:g.30199047A>C	GRCh37
NC_000019.8:g.34890887A>C	NCBI36
NG_031970.1:g.12650T>G
NG_031970.2:g.12650T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614091.5:c.160+114T>G	ENSP00000482097.2:n.160+114T>G
ENST00000623113.3:c.160+114T>G	ENSP00000485413.2:n.160+114T>G
ENST00000323670.14:c.160+114T>G MANE Select	ENSP00000313332.9:n.160+114T>G
ENST00000323670.13:c.160+114T>G	ENSP00000313332.8:n.160+114T>G
ENST00000342680.5:c.160+114T>G	ENSP00000345497.5:n.160+114T>G
ENST00000392275.1:n.552-5163T>G
ENST00000392276.1:c.-32-5163T>G	ENSP00000376102.1:n.-32-5163T>G
ENST00000392278.2:c.193+114T>G	ENSP00000376103.2:n.193+114T>G
ENST00000591243.1:c.160+114T>G	ENSP00000467516.1:n.160+114T>G
ENST00000592153.5:c.160+114T>G	ENSP00000467117.1:n.160+114T>G
ENST00000614091.4:c.160+114T>G	ENSP00000482097.1:n.160+114T>G
ENST00000623113.1:c.-32-5163T>G	ENSP00000485413.1:n.-32-5163T>G
NM_001031726.3:c.193+114T>G	NP_001026896.2:n.193+114T>G
NM_001256046.1:c.160+114T>G	NP_001242975.1:n.160+114T>G
NM_001256047.1:c.160+114T>G	NP_001242976.1:n.160+114T>G
NM_001282929.1:c.-32-5163T>G	NP_001269858.1:n.-32-5163T>G
NM_001282930.1:c.-32-5163T>G	NP_001269859.1:n.-32-5163T>G
NM_001282931.1:c.-154+114T>G	NP_001269860.1:n.-154+114T>G
NM_031448.4:c.160+114T>G	NP_113636.2:n.160+114T>G
XM_024451734.1:c.322+114T>G	XP_024307502.1:n.322+114T>G
XM_024451735.1:c.160+114T>G	XP_024307503.1:n.160+114T>G
XM_024451736.1:c.160+114T>G	XP_024307504.1:n.160+114T>G
XM_024451737.1:c.160+114T>G	XP_024307505.1:n.160+114T>G
XM_024451738.1:c.160+114T>G	XP_024307506.1:n.160+114T>G
NM_001256046.2:c.160+114T>G	NP_001242975.1:n.160+114T>G
NM_001282930.2:c.-32-5163T>G	NP_001269859.1:n.-32-5163T>G
NM_001282931.2:c.-154+114T>G	NP_001269860.1:n.-154+114T>G
NM_031448.6:c.160+114T>G MANE Select	NP_113636.2:n.160+114T>G
NM_001031726.4:c.160+114T>G	NP_001026896.3:n.160+114T>G
NM_001256046.3:c.160+114T>G	NP_001242975.1:n.160+114T>G
NM_001256047.2:c.160+114T>G	NP_001242976.1:n.160+114T>G
NM_001282930.3:c.-32-5163T>G	NP_001269859.1:n.-32-5163T>G
NM_001282931.3:c.-154+114T>G	NP_001269860.1:n.-154+114T>G