Canonical Allele Identifier: CA1946792882

Gene: MTG1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133412121_133412122delinsGT , CM000672.2:g.133412121_133412122delinsGT	GRCh38
NC_000010.10:g.135225625_135225626delinsGT , CM000672.1:g.135225625_135225626delinsGT	GRCh37
NC_000010.9:g.135075615_135075616delinsGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317502.11:c.753-7359_753-7358delinsGT MANE Select	ENSP00000323047.6:n.753-7359_753-7358delinsGT
ENST00000468317.3:c.*677-7359_*677-7358delinsGT	ENSP00000436767.2:n.*677-7359_*677-7358delinsGT
ENST00000317502.10:c.753-7359_753-7358delinsGT	ENSP00000323047.6:n.753-7359_753-7358delinsGT
ENST00000432508.3:c.600-7359_600-7358delinsGT	ENSP00000393480.2:n.600-7359_600-7358delinsGT
ENST00000460848.5:n.1336-7359_1336-7358delinsGT
ENST00000468317.2:c.768-7359_768-7358delinsGT	ENSP00000436767.1:n.768-7359_768-7358delinsGT
ENST00000473735.1:n.1607-7359_1607-7358delinsGT
ENST00000477902.6:c.630-7359_630-7358delinsGT	ENSP00000475596.1:n.630-7359_630-7358delinsGT
NM_138384.2:c.753-7359_753-7358delinsGT	NP_612393.2:n.753-7359_753-7358delinsGT
NM_138384.3:c.753-7359_753-7358delinsGT	NP_612393.2:n.753-7359_753-7358delinsGT
NM_138384.4:c.753-7359_753-7358delinsGT MANE Select	NP_612393.2:n.753-7359_753-7358delinsGT