Canonical Allele Identifier: CA4426714

Gene: RINT1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.105555159C>T , CM000669.2:g.105555159C>T	GRCh38
NC_000007.13:g.105195606C>T , CM000669.1:g.105195606C>T	GRCh37
NC_000007.12:g.104982842C>T	NCBI36
NG_051951.1:g.28079C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021930.6:c.1603C>T MANE Select	NP_068749.3:p.Arg535Ter
ENST00000257700.7:c.1603C>T MANE Select	ENSP00000257700.2:p.Arg535Ter
NM_001346599.1:c.1369C>T	NP_001333528.1:p.Arg457Ter
NM_001346599.2:c.1369C>T	NP_001333528.1:p.Arg457Ter
NM_001346600.1:c.580C>T	NP_001333529.1:p.Arg194Ter
NM_001346600.2:c.580C>T	NP_001333529.1:p.Arg194Ter
NM_001346601.1:c.679C>T	NP_001333530.1:p.Arg227Ter
NM_001346601.2:c.679C>T	NP_001333530.1:p.Arg227Ter
NM_001346603.1:c.580C>T	NP_001333532.1:p.Arg194Ter
NM_001346603.2:c.580C>T	NP_001333532.1:p.Arg194Ter
NM_021930.4:c.1603C>T	NP_068749.3:p.Arg535Ter
NM_021930.5:c.1603C>T	NP_068749.3:p.Arg535Ter
NR_144478.1:n.1706+3452C>T
NR_144478.2:n.1586+3452C>T
ENST00000257700.6:c.1603C>T	ENSP00000257700.2:p.Arg535Ter
ENST00000474123.1:n.607C>T
ENST00000497979.5:c.*1208C>T	ENSP00000420582.1:n.*1208C>T
XM_005250524.2:c.580C>T	XP_005250581.1:p.Arg194Ter
XM_005250524.4:c.580C>T	XP_005250581.1:p.Arg194Ter
XM_011516458.1:c.580C>T	XP_011514760.1:p.Arg194Ter
XM_011516458.3:c.580C>T	XP_011514760.1:p.Arg194Ter
XM_024446855.1:c.1603C>T	XP_024302623.1:p.Arg535Ter
XM_024446856.1:c.580C>T	XP_024302624.1:p.Arg194Ter
XR_927507.1:n.1618+3452C>T