Canonical Allele Identifier: CA2814087739

Gene: C19orf12

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.29702977_29702978dup , CM000681.2:g.29702977_29702978dup	GRCh38
NC_000019.9:g.30193884_30193885dup , CM000681.1:g.30193884_30193885dup	GRCh37
NC_000019.8:g.34885724_34885725dup	NCBI36
NG_031970.1:g.17817_17818dup
NG_031970.2:g.17817_17818dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614091.5:c.165_166dup
ENST00000623113.3:c.165_166dup
ENST00000323670.14:c.165_166dup
ENST00000323670.13:c.165_166dup
ENST00000342680.5:c.*79_*80dup
ENST00000392275.1:n.556_557dup
ENST00000392276.1:c.-28_-27dup
ENST00000392278.2:c.198_199dup
ENST00000591243.1:c.165_166dup
ENST00000592153.5:c.165_166dup
ENST00000614091.4:c.165_166dup
ENST00000623113.1:c.-28_-27dup
NM_001031726.3:c.198_199dup
NM_001256046.1:c.165_166dup
NM_001256047.1:c.165_166dup
NM_001282929.1:c.-28_-27dup
NM_001282930.1:c.-28_-27dup
NM_001282931.1:c.-28_-27dup
NM_031448.4:c.165_166dup
XM_024451734.1:c.327_328dup
XM_024451735.1:c.165_166dup
XM_024451736.1:c.165_166dup
XM_024451737.1:c.165_166dup
XM_024451738.1:c.165_166dup
NM_001256046.2:c.165_166dup
NM_001282930.2:c.-28_-27dup
NM_001282931.2:c.-28_-27dup
NM_031448.6:c.165_166dup
NM_001031726.4:c.165_166dup
NM_001256046.3:c.165_166dup
NM_001256047.2:c.165_166dup
NM_001282930.3:c.-28_-27dup
NM_001282931.3:c.-28_-27dup