Canonical Allele Identifier: CA2581867881

Gene: MYRIP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39967143T>G , CM000665.2:g.39967143T>G	GRCh38
NC_000003.11:g.40008634T>G , CM000665.1:g.40008634T>G	GRCh37
NC_000003.10:g.39983638T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000302541.11:c.110+66217T>G MANE Select	ENSP00000301972.6:n.110+66217T>G
ENST00000302541.10:c.110+66217T>G	ENSP00000301972.6:n.110+66217T>G
ENST00000396217.7:c.-21+66217T>G	ENSP00000379519.3:n.-21+66217T>G
ENST00000425621.5:c.110+66217T>G	ENSP00000389323.1:n.110+66217T>G
ENST00000444716.5:c.110+66217T>G	ENSP00000398665.1:n.110+66217T>G
ENST00000458292.5:c.110+66217T>G	ENSP00000413392.1:n.110+66217T>G
ENST00000458441.5:c.110+66217T>G	ENSP00000400916.1:n.110+66217T>G
ENST00000475082.5:n.369+66217T>G
NM_001284423.1:c.110+66217T>G	NP_001271352.1:n.110+66217T>G
NM_001284424.1:c.110+66217T>G	NP_001271353.1:n.110+66217T>G
NM_001284425.1:c.-21+66217T>G	NP_001271354.1:n.-21+66217T>G
NM_015460.3:c.110+66217T>G	NP_056275.2:n.110+66217T>G
NR_104316.1:n.397+66217T>G
XM_011533575.1:c.110+66217T>G	XP_011531877.1:n.110+66217T>G
NM_015460.4:c.110+66217T>G MANE Select	NP_056275.2:n.110+66217T>G
NM_001284424.2:c.110+66217T>G	NP_001271353.1:n.110+66217T>G
NR_104316.2:n.448+66217T>G
NM_001284423.2:c.110+66217T>G	NP_001271352.1:n.110+66217T>G
NM_001284425.2:c.-21+66217T>G	NP_001271354.1:n.-21+66217T>G