Canonical Allele Identifier: CA1946793013

Gene: MTG1

Linked Data

• dbSNP Id: rs1850058377

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133412292_133412303del , CM000672.2:g.133412292_133412303del	GRCh38
NC_000010.10:g.135225796_135225807del , CM000672.1:g.135225796_135225807del	GRCh37
NC_000010.9:g.135075786_135075797del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317502.11:c.753-7188_753-7177del MANE Select	ENSP00000323047.6:n.753-7188_753-7177del
ENST00000468317.3:c.*677-7188_*677-7177del	ENSP00000436767.2:n.*677-7188_*677-7177del
ENST00000317502.10:c.753-7188_753-7177del	ENSP00000323047.6:n.753-7188_753-7177del
ENST00000432508.3:c.600-7188_600-7177del	ENSP00000393480.2:n.600-7188_600-7177del
ENST00000460848.5:n.1336-7188_1336-7177del
ENST00000468317.2:c.768-7188_768-7177del	ENSP00000436767.1:n.768-7188_768-7177del
ENST00000473735.1:n.1607-7188_1607-7177del
ENST00000477902.6:c.630-7188_630-7177del	ENSP00000475596.1:n.630-7188_630-7177del
NM_138384.2:c.753-7188_753-7177del	NP_612393.2:n.753-7188_753-7177del
NM_138384.3:c.753-7188_753-7177del	NP_612393.2:n.753-7188_753-7177del
NM_138384.4:c.753-7188_753-7177del MANE Select	NP_612393.2:n.753-7188_753-7177del