Canonical Allele Identifier: CA2330916083

Gene: C19orf12

Linked Data

• dbSNP Id: rs1972505476

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29708633_29708635del , CM000681.2:g.29708633_29708635del	GRCh38
NC_000019.9:g.30199540_30199542del , CM000681.1:g.30199540_30199542del	GRCh37
NC_000019.8:g.34891380_34891382del	NCBI36
NG_031970.1:g.12161_12163del
NG_031970.2:g.12161_12163del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614091.5:c.-10-206_-10-204del	ENSP00000482097.2:n.-10-206_-10-204del
ENST00000623113.3:c.-10-206_-10-204del	ENSP00000485413.2:n.-10-206_-10-204del
ENST00000323670.14:c.-10-206_-10-204del MANE Select	ENSP00000313332.9:n.-10-206_-10-204del
ENST00000323670.13:c.-10-206_-10-204del	ENSP00000313332.8:n.-10-206_-10-204del
ENST00000342680.5:c.-10-206_-10-204del	ENSP00000345497.5:n.-10-206_-10-204del
ENST00000392275.1:n.552-5652_552-5650del
ENST00000392276.1:c.-32-5652_-32-5650del	ENSP00000376102.1:n.-32-5652_-32-5650del
ENST00000392278.2:c.24-206_24-204del	ENSP00000376103.2:n.24-206_24-204del
ENST00000591243.1:c.-216_-214del	ENSP00000467516.1:n.-216_-214del
ENST00000592153.5:c.-10-206_-10-204del	ENSP00000467117.1:n.-10-206_-10-204del
ENST00000614091.4:c.-10-206_-10-204del	ENSP00000482097.1:n.-10-206_-10-204del
ENST00000623113.1:c.-32-5652_-32-5650del	ENSP00000485413.1:n.-32-5652_-32-5650del
NM_001031726.3:c.24-206_24-204del	NP_001026896.2:n.24-206_24-204del
NM_001256046.1:c.-10-206_-10-204del	NP_001242975.1:n.-10-206_-10-204del
NM_001256047.1:c.-10-206_-10-204del	NP_001242976.1:n.-10-206_-10-204del
NM_001282929.1:c.-32-5652_-32-5650del	NP_001269858.1:n.-32-5652_-32-5650del
NM_001282930.1:c.-32-5652_-32-5650del	NP_001269859.1:n.-32-5652_-32-5650del
NM_001282931.1:c.-323-206_-323-204del	NP_001269860.1:n.-323-206_-323-204del
NM_031448.4:c.-10-206_-10-204del	NP_113636.2:n.-10-206_-10-204del
XM_024451734.1:c.152+55_152+57del	XP_024307502.1:n.152+55_152+57del
XM_024451735.1:c.-10-206_-10-204del	XP_024307503.1:n.-10-206_-10-204del
XM_024451736.1:c.-10-206_-10-204del	XP_024307504.1:n.-10-206_-10-204del
XM_024451737.1:c.-10-206_-10-204del	XP_024307505.1:n.-10-206_-10-204del
XM_024451738.1:c.-10-206_-10-204del	XP_024307506.1:n.-10-206_-10-204del
NM_001256046.2:c.-10-206_-10-204del	NP_001242975.1:n.-10-206_-10-204del
NM_001282930.2:c.-32-5652_-32-5650del	NP_001269859.1:n.-32-5652_-32-5650del
NM_001282931.2:c.-323-206_-323-204del	NP_001269860.1:n.-323-206_-323-204del
NM_031448.6:c.-10-206_-10-204del MANE Select	NP_113636.2:n.-10-206_-10-204del
NM_001031726.4:c.-10-206_-10-204del	NP_001026896.3:n.-10-206_-10-204del
NM_001256046.3:c.-10-206_-10-204del	NP_001242975.1:n.-10-206_-10-204del
NM_001256047.2:c.-10-206_-10-204del	NP_001242976.1:n.-10-206_-10-204del
NM_001282930.3:c.-32-5652_-32-5650del	NP_001269859.1:n.-32-5652_-32-5650del
NM_001282931.3:c.-323-206_-323-204del	NP_001269860.1:n.-323-206_-323-204del