Canonical Allele Identifier: CA1979335423

Gene: RNASEH2C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65720101G= , CM000673.2:g.65720101G=	GRCh38
NC_000011.9:g.65487572G= , CM000673.1:g.65487572G=	GRCh37
NC_000011.8:g.65244148G=	NCBI36
NG_008976.2:g.5838C= , LRG_280:g.5838C=
NG_033057.1:g.13100G=

Transcript Alleles

HGVS	Amino-acid Change
NM_032193.4:c.412C= MANE Select	NP_115569.2:p.Pro138=
ENST00000308418.10:c.412C= MANE Select	ENSP00000308193.5:p.Pro138=
NM_032193.3:c.412C= , LRG_280t1:c.412C=	NP_115569.2:p.Pro138=
ENST00000308418.8:c.412C=	ENSP00000308193.4:p.Pro138=
ENST00000527610.1:c.412C=	ENSP00000432897.1:p.Pro138=
ENST00000528220.1:c.163C=	ENSP00000431555.1:p.Pro55=
ENST00000528220.2:n.641C=
ENST00000530192.1:n.529C=
ENST00000531596.5:c.393C=
ENST00000531596.6:c.412C=	ENSP00000435717.2:p.Pro138=
ENST00000533698.5:c.291C=
ENST00000534482.5:c.306C=
ENST00000534482.6:c.412C=	ENSP00000432081.2:p.Pro138=
ENST00000642430.1:n.305C=
ENST00000643214.1:n.486C=
ENST00000644142.1:c.412C=	ENSP00000493695.1:p.Pro138=
ENST00000644198.1:n.309C=
ENST00000646597.1:n.349C=