Canonical Allele Identifier: CA1860350026

Gene: RMI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84002350A= , CM000671.2:g.84002350A=	GRCh38
NC_000009.11:g.86617265A= , CM000671.1:g.86617265A=	GRCh37
NC_000009.10:g.85807085A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445877.6:c.1364A= MANE Select	ENSP00000402433.2:p.Asn455=
ENST00000325875.7:c.1364A=	ENSP00000317039.3:p.Asn455=
ENST00000615118.1:c.1363A=	ENSP00000483816.1:p.Ile455=
NM_024945.2:c.1364A=	NP_079221.2:p.Asn455=
XM_005252211.1:c.1364A=	XP_005252268.1:p.Asn455=
XM_005252213.1:c.1364A=	XP_005252270.1:p.Asn455=
XM_011519034.1:c.1364A=	XP_011517336.1:p.Asn455=
NM_001358291.1:c.1364A=	NP_001345220.1:p.Asn455=
NM_001358292.1:c.1364A=	NP_001345221.1:p.Asn455=
NM_001358293.1:c.1364A=	NP_001345222.1:p.Asn455=
NM_001358294.1:c.1364A=	NP_001345223.1:p.Asn455=
XM_017015140.1:c.1364A=	XP_016870629.1:p.Asn455=
NM_001358291.2:c.1364A= MANE Select	NP_001345220.1:p.Asn455=
NM_001358292.2:c.1364A=	NP_001345221.1:p.Asn455=
NM_001358293.2:c.1364A=	NP_001345222.1:p.Asn455=
NM_024945.3:c.1364A=	NP_079221.2:p.Asn455=
NM_001358294.2:c.1364A=	NP_001345223.1:p.Asn455=