Canonical Allele Identifier: CA2330915951

Gene: C19orf12

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29708307_29708309delinsCCT , CM000681.2:g.29708307_29708309delinsCCT	GRCh38
NC_000019.9:g.30199214_30199216delinsCCT , CM000681.1:g.30199214_30199216delinsCCT	GRCh37
NC_000019.8:g.34891054_34891056delinsCCT	NCBI36
NG_031970.1:g.12481_12483delinsAGG
NG_031970.2:g.12481_12483delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614091.5:c.105_107delinsAGG	ENSP00000482097.2:p.Thr35=
ENST00000623113.3:c.105_107delinsAGG	ENSP00000485413.2:p.Thr35=
ENST00000323670.14:c.105_107delinsAGG MANE Select	ENSP00000313332.9:p.Thr35=
ENST00000323670.13:c.105_107delinsAGG	ENSP00000313332.8:p.Thr35=
ENST00000342680.5:c.105_107delinsAGG	ENSP00000345497.5:p.Thr35=
ENST00000392275.1:n.552-5332_552-5330delinsAGG
ENST00000392276.1:c.-32-5332_-32-5330delinsAGG	ENSP00000376102.1:n.-32-5332_-32-5330delinsAGG
ENST00000392278.2:c.138_140delinsAGG	ENSP00000376103.2:p.Thr46=
ENST00000591243.1:c.105_107delinsAGG	ENSP00000467516.1:p.Thr35=
ENST00000592153.5:c.105_107delinsAGG	ENSP00000467117.1:p.Thr35=
ENST00000614091.4:c.105_107delinsAGG	ENSP00000482097.1:p.Thr35=
ENST00000623113.1:c.-32-5332_-32-5330delinsAGG	ENSP00000485413.1:n.-32-5332_-32-5330delinsAGG
NM_001031726.3:c.138_140delinsAGG	NP_001026896.2:p.Thr46=
NM_001256046.1:c.105_107delinsAGG	NP_001242975.1:p.Thr35=
NM_001256047.1:c.105_107delinsAGG	NP_001242976.1:p.Thr35=
NM_001282929.1:c.-32-5332_-32-5330delinsAGG	NP_001269858.1:n.-32-5332_-32-5330delinsAGG
NM_001282930.1:c.-32-5332_-32-5330delinsAGG	NP_001269859.1:n.-32-5332_-32-5330delinsAGG
NM_001282931.1:c.-209_-207delinsAGG	NP_001269860.1:n.-209_-207delinsAGG
NM_031448.4:c.105_107delinsAGG	NP_113636.2:p.Thr35=
XM_024451734.1:c.267_269delinsAGG	XP_024307502.1:p.Thr89=
XM_024451735.1:c.105_107delinsAGG	XP_024307503.1:p.Thr35=
XM_024451736.1:c.105_107delinsAGG	XP_024307504.1:p.Thr35=
XM_024451737.1:c.105_107delinsAGG	XP_024307505.1:p.Thr35=
XM_024451738.1:c.105_107delinsAGG	XP_024307506.1:p.Thr35=
NM_001256046.2:c.105_107delinsAGG	NP_001242975.1:p.Thr35=
NM_001282930.2:c.-32-5332_-32-5330delinsAGG	NP_001269859.1:n.-32-5332_-32-5330delinsAGG
NM_001282931.2:c.-209_-207delinsAGG	NP_001269860.1:n.-209_-207delinsAGG
NM_031448.6:c.105_107delinsAGG MANE Select	NP_113636.2:p.Thr35=
NM_001031726.4:c.105_107delinsAGG	NP_001026896.3:p.Thr35=
NM_001256046.3:c.105_107delinsAGG	NP_001242975.1:p.Thr35=
NM_001256047.2:c.105_107delinsAGG	NP_001242976.1:p.Thr35=
NM_001282930.3:c.-32-5332_-32-5330delinsAGG	NP_001269859.1:n.-32-5332_-32-5330delinsAGG
NM_001282931.3:c.-209_-207delinsAGG	NP_001269860.1:n.-209_-207delinsAGG