Canonical Allele Identifier: CA1979335377

Gene: RNASEH2C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65720085T= , CM000673.2:g.65720085T=	GRCh38
NC_000011.9:g.65487556T= , CM000673.1:g.65487556T=	GRCh37
NC_000011.8:g.65244132T=	NCBI36
NG_008976.2:g.5854A= , LRG_280:g.5854A=
NG_033057.1:g.13084T=

Transcript Alleles

HGVS	Amino-acid Change
NM_032193.4:c.428A= MANE Select	NP_115569.2:p.Lys143=
ENST00000308418.10:c.428A= MANE Select	ENSP00000308193.5:p.Lys143=
NM_032193.3:c.428A= , LRG_280t1:c.428A=	NP_115569.2:p.Lys143=
ENST00000308418.8:c.428A=	ENSP00000308193.4:p.Lys143=
ENST00000527610.1:c.428A=	ENSP00000432897.1:p.Lys143=
ENST00000528220.1:c.179A=	ENSP00000431555.1:p.Lys60=
ENST00000528220.2:n.657A=
ENST00000530192.1:n.545A=
ENST00000531596.5:c.409A=
ENST00000531596.6:c.428A=	ENSP00000435717.2:p.Lys143=
ENST00000533698.5:c.307A=
ENST00000534482.5:c.322A=
ENST00000534482.6:c.428A=	ENSP00000432081.2:p.Lys143=
ENST00000642430.1:n.321A=
ENST00000643214.1:n.502A=
ENST00000644142.1:c.428A=	ENSP00000493695.1:p.Lys143=
ENST00000644198.1:n.325A=
ENST00000646597.1:n.365A=