Canonical Allele Identifier: CA2346769614

Gene: MAVS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857552_3857557delinsTCCCCC , CM000682.2:g.3857552_3857557delinsTCCCCC	GRCh38
NC_000020.10:g.3838199_3838204delinsTCCCCC , CM000682.1:g.3838199_3838204delinsTCCCCC	GRCh37
NC_000020.9:g.3786199_3786204delinsTCCCCC	NCBI36
NG_030028.1:g.15754_15759delinsTCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.118-83_118-78delinsTCCCCC MANE Select	ENSP00000401980.2:n.118-83_118-78delinsTCCCCC
ENST00000416600.6:c.-132+2811_-132+2816delinsTCCCCC	ENSP00000413749.2:n.-132+2811_-132+2816delinsTCCCCC
ENST00000428216.3:c.118-83_118-78delinsTCCCCC	ENSP00000401980.2:n.118-83_118-78delinsTCCCCC
NM_001206491.1:c.-132+2811_-132+2816delinsTCCCCC	NP_001193420.1:n.-132+2811_-132+2816delinsTCCCCC
NM_020746.4:c.118-83_118-78delinsTCCCCC	NP_065797.2:n.118-83_118-78delinsTCCCCC
NR_037921.1:n.290-83_290-78delinsTCCCCC
NM_020746.5:c.118-83_118-78delinsTCCCCC MANE Select	NP_065797.2:n.118-83_118-78delinsTCCCCC
NR_037921.2:n.255-83_255-78delinsTCCCCC
NM_001206491.2:c.-132+2811_-132+2816delinsTCCCCC	NP_001193420.1:n.-132+2811_-132+2816delinsTCCCCC
NM_001385663.1:c.-430-83_-430-78delinsTCCCCC	NP_001372592.1:n.-430-83_-430-78delinsTCCCCC