Canonical Allele Identifier: CA10620309

Gene: MATR3

Linked Data

• ClinVar Variation Id: 351128
• ClinVar RCV Id: RCV000304798
• dbSNP Id: rs886059990
• MyVariant Identifiers: chr5:g.138657729T>G (hg19) ; chr5:g.139322040T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139322040T>G , CM000667.2:g.139322040T>G	GRCh38
NC_000005.9:g.138657729T>G , CM000667.1:g.138657729T>G	GRCh37
NC_000005.8:g.138685628T>G	NCBI36
NG_012846.1:g.52938T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394805.8:c.1734+11T>G MANE Select	ENSP00000378284.3:n.1734+11T>G
ENST00000618441.5:c.1734+11T>G	ENSP00000482895.1:n.1734+11T>G
ENST00000361059.7:c.1734+11T>G	ENSP00000354346.4:n.1734+11T>G
ENST00000394800.6:c.1734+11T>G	ENSP00000378279.2:n.1734+11T>G
ENST00000394805.7:c.1734+11T>G	ENSP00000378284.3:n.1734+11T>G
ENST00000502422.5:n.1043+11T>G
ENST00000502499.5:c.720+11T>G	ENSP00000426030.1:n.720+11T>G
ENST00000502929.5:c.1734+11T>G	ENSP00000422319.1:n.1734+11T>G
ENST00000502944.1:n.225+11T>G
ENST00000503811.5:c.870+11T>G	ENSP00000423587.1:n.870+11T>G
ENST00000504203.5:c.720+11T>G	ENSP00000421218.1:n.720+11T>G
ENST00000504643.5:n.2165+11T>G
ENST00000505625.5:n.5454+11T>G
ENST00000509990.5:c.1734+11T>G	ENSP00000423533.1:n.1734+11T>G
ENST00000510056.5:c.1734+11T>G	ENSP00000426743.1:n.1734+11T>G
ENST00000618441.4:c.1734+11T>G	ENSP00000482895.1:n.1734+11T>G
ENST00000620916.2:c.114-729T>G	ENSP00000480093.1:n.114-729T>G
NM_001194954.1:c.1734+11T>G	NP_001181883.1:n.1734+11T>G
NM_001194955.1:c.1734+11T>G	NP_001181884.1:n.1734+11T>G
NM_001194956.1:c.870+11T>G	NP_001181885.1:n.870+11T>G
NM_001282278.1:c.720+11T>G	NP_001269207.1:n.720+11T>G
NM_018834.5:c.1734+11T>G	NP_061322.2:n.1734+11T>G
NM_199189.2:c.1734+11T>G	NP_954659.1:n.1734+11T>G
NM_018834.6:c.1734+11T>G MANE Select	NP_061322.2:n.1734+11T>G
NM_001194954.2:c.1734+11T>G	NP_001181883.1:n.1734+11T>G
NM_001194955.2:c.1734+11T>G	NP_001181884.1:n.1734+11T>G
NM_001194956.2:c.870+11T>G	NP_001181885.1:n.870+11T>G
NM_001282278.2:c.720+11T>G	NP_001269207.1:n.720+11T>G
NM_199189.3:c.1734+11T>G	NP_954659.1:n.1734+11T>G
NM_001400441.1:c.1734+11T>G	NP_001387370.1:n.1734+11T>G
NM_001400442.1:c.1734+11T>G	NP_001387371.1:n.1734+11T>G
NM_001400443.1:c.1734+11T>G	NP_001387372.1:n.1734+11T>G
NM_001400444.1:c.1734+11T>G	NP_001387373.1:n.1734+11T>G
NM_001400445.1:c.1734+11T>G	NP_001387374.1:n.1734+11T>G
NM_001400447.1:c.1734+11T>G	NP_001387376.1:n.1734+11T>G
NM_001400448.1:c.1734+11T>G	NP_001387377.1:n.1734+11T>G
NM_001400450.1:c.1734+11T>G	NP_001387379.1:n.1734+11T>G
NM_001400451.1:c.1734+11T>G	NP_001387380.1:n.1734+11T>G
NM_001400452.1:c.1734+11T>G	NP_001387381.1:n.1734+11T>G
NM_001400453.1:c.1734+11T>G	NP_001387382.1:n.1734+11T>G
NM_001400454.1:c.1734+11T>G	NP_001387383.1:n.1734+11T>G
NM_001400455.1:c.1734+11T>G	NP_001387384.1:n.1734+11T>G
NM_001400456.1:c.1734+11T>G	NP_001387385.1:n.1734+11T>G
NM_001400457.1:c.1734+11T>G	NP_001387386.1:n.1734+11T>G
NM_001400458.1:c.1734+11T>G	NP_001387387.1:n.1734+11T>G
NM_001400459.1:c.873+11T>G	NP_001387388.1:n.873+11T>G
NM_001400460.1:c.720+11T>G	NP_001387389.1:n.720+11T>G
NM_001400461.1:c.834+11T>G	NP_001387390.1:n.834+11T>G
NM_001400462.1:c.720+11T>G	NP_001387391.1:n.720+11T>G
NM_001400463.1:c.720+11T>G	NP_001387392.1:n.720+11T>G
NM_001400464.1:c.720+11T>G	NP_001387393.1:n.720+11T>G
NM_001400465.1:c.720+11T>G	NP_001387394.1:n.720+11T>G
NM_001400466.1:c.720+11T>G	NP_001387395.1:n.720+11T>G
NM_001400467.1:c.720+11T>G	NP_001387396.1:n.720+11T>G