Canonical Allele Identifier: CA1359241782

Gene: MYRIP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.40055127G= , CM000665.2:g.40055127G=	GRCh38
NC_000003.11:g.40096618G= , CM000665.1:g.40096618G=	GRCh37
NC_000003.10:g.40071622G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302541.11:c.332+10856G= MANE Select	ENSP00000301972.6:n.332+10856G=
ENST00000302541.10:c.332+10856G=	ENSP00000301972.6:n.332+10856G=
ENST00000396217.7:c.202+10856G=	ENSP00000379519.3:n.202+10856G=
ENST00000425621.5:c.332+10856G=	ENSP00000389323.1:n.332+10856G=
ENST00000444716.5:c.332+10856G=	ENSP00000398665.1:n.332+10856G=
ENST00000458292.5:c.332+10856G=	ENSP00000413392.1:n.332+10856G=
ENST00000458441.5:c.332+10856G=	ENSP00000400916.1:n.332+10856G=
ENST00000475082.5:n.591+10856G=
NM_001284423.1:c.332+10856G=	NP_001271352.1:n.332+10856G=
NM_001284424.1:c.332+10856G=	NP_001271353.1:n.332+10856G=
NM_001284425.1:c.202+10856G=	NP_001271354.1:n.202+10856G=
NM_015460.3:c.332+10856G=	NP_056275.2:n.332+10856G=
NR_104316.1:n.619+10856G=
XM_011533575.1:c.332+10856G=	XP_011531877.1:n.332+10856G=
NM_015460.4:c.332+10856G= MANE Select	NP_056275.2:n.332+10856G=
NM_001284424.2:c.332+10856G=	NP_001271353.1:n.332+10856G=
NR_104316.2:n.670+10856G=
NM_001284423.2:c.332+10856G=	NP_001271352.1:n.332+10856G=
NM_001284425.2:c.202+10856G=	NP_001271354.1:n.202+10856G=