Canonical Allele Identifier: CA2346769796

Gene: MAVS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3857896_3857898delinsTTC , CM000682.2:g.3857896_3857898delinsTTC	GRCh38
NC_000020.10:g.3838543_3838545delinsTTC , CM000682.1:g.3838543_3838545delinsTTC	GRCh37
NC_000020.9:g.3786543_3786545delinsTTC	NCBI36
NG_030028.1:g.16098_16100delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428216.4:c.292+87_292+89delinsTTC MANE Select	ENSP00000401980.2:n.292+87_292+89delinsTTC
ENST00000416600.6:c.-132+3155_-132+3157delinsTTC	ENSP00000413749.2:n.-132+3155_-132+3157delinsTTC
ENST00000428216.3:c.292+87_292+89delinsTTC	ENSP00000401980.2:n.292+87_292+89delinsTTC
NM_001206491.1:c.-132+3155_-132+3157delinsTTC	NP_001193420.1:n.-132+3155_-132+3157delinsTTC
NM_020746.4:c.292+87_292+89delinsTTC	NP_065797.2:n.292+87_292+89delinsTTC
NR_037921.1:n.464+87_464+89delinsTTC
NM_020746.5:c.292+87_292+89delinsTTC MANE Select	NP_065797.2:n.292+87_292+89delinsTTC
NR_037921.2:n.429+87_429+89delinsTTC
NM_001206491.2:c.-132+3155_-132+3157delinsTTC	NP_001193420.1:n.-132+3155_-132+3157delinsTTC
NM_001385663.1:c.-256+87_-256+89delinsTTC	NP_001372592.1:n.-256+87_-256+89delinsTTC