Canonical Allele Identifier: CA691017896

Gene: MSRB3

Linked Data

• dbSNP Id: rs1221739658
• MyVariant Identifiers: chr12:g.65842313_65842319del (hg19) ; chr12:g.65448533_65448539del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65448536_65448542del , CM000674.2:g.65448536_65448542del	GRCh38
NC_000012.11:g.65842316_65842322del , CM000674.1:g.65842316_65842322del	GRCh37
NC_000012.10:g.64128583_64128589del	NCBI36
NG_023441.1:g.174894_174900del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308259.10:c.293-5192_293-5186del MANE Select	ENSP00000312274.6:n.293-5192_293-5186del
ENST00000355192.8:c.314-5192_314-5186del	ENSP00000347324.3:n.314-5192_314-5186del
ENST00000642404.1:c.293-5192_293-5186del	ENSP00000496008.1:n.293-5192_293-5186del
ENST00000642411.1:c.293-5192_293-5186del	ENSP00000494265.1:n.293-5192_293-5186del
ENST00000646299.1:c.293-5192_293-5186del	ENSP00000494941.1:n.293-5192_293-5186del
ENST00000647481.1:c.98-5192_98-5186del	ENSP00000496162.1:n.98-5192_98-5186del
ENST00000308259.9:c.293-5192_293-5186del	ENSP00000312274.5:n.293-5192_293-5186del
ENST00000355192.7:c.314-5192_314-5186del	ENSP00000347324.3:n.314-5192_314-5186del
ENST00000446731.2:c.168-5192_168-5186del
ENST00000535143.1:n.132-5192_132-5186del
ENST00000535239.5:c.293-5192_293-5186del	ENSP00000445843.1:n.293-5192_293-5186del
ENST00000535664.5:c.293-5192_293-5186del	ENSP00000441650.1:n.293-5192_293-5186del
ENST00000538045.5:c.293-5192_293-5186del	ENSP00000442620.1:n.293-5192_293-5186del
ENST00000540804.5:c.314-5192_314-5186del	ENSP00000437623.1:n.314-5192_314-5186del
ENST00000541189.5:c.339-5192_339-5186del
ENST00000541897.5:c.*119-5192_*119-5186del	ENSP00000445051.1:n.*119-5192_*119-5186del
ENST00000614640.4:c.293-5192_293-5186del	ENSP00000481483.1:n.293-5192_293-5186del
NM_001031679.2:c.293-5192_293-5186del	NP_001026849.1:n.293-5192_293-5186del
NM_001193460.1:c.293-5192_293-5186del	NP_001180389.1:n.293-5192_293-5186del
NM_001193461.1:c.293-5192_293-5186del	NP_001180390.1:n.293-5192_293-5186del
NM_198080.3:c.314-5192_314-5186del	NP_932346.1:n.314-5192_314-5186del
XM_024448918.1:c.293-5192_293-5186del	XP_024304686.1:n.293-5192_293-5186del
XM_024448919.1:c.293-5192_293-5186del	XP_024304687.1:n.293-5192_293-5186del
XM_024448920.1:c.293-5192_293-5186del	XP_024304688.1:n.293-5192_293-5186del
XM_024448921.1:c.293-5192_293-5186del	XP_024304689.1:n.293-5192_293-5186del
NM_001031679.3:c.293-5192_293-5186del MANE Select	NP_001026849.1:n.293-5192_293-5186del
NM_001193460.2:c.293-5192_293-5186del	NP_001180389.1:n.293-5192_293-5186del
NM_198080.4:c.314-5192_314-5186del	NP_932346.1:n.314-5192_314-5186del
NM_001193461.2:c.293-5192_293-5186del	NP_001180390.1:n.293-5192_293-5186del