Canonical Allele Identifier: CA934184968
Gene: MTG1 HGNC NCBI

Linked Data

dbSNP Id: rs1850058004

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133412261A>T , CM000672.2:g.133412261A>T GRCh38
NC_000010.10:g.135225765A>T , CM000672.1:g.135225765A>T GRCh37
NC_000010.9:g.135075755A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000317502.11:c.753-7219A>T MANE Select ENSP00000323047.6:n.753-7219A>T
ENST00000468317.3:c.*677-7219A>T ENSP00000436767.2:n.*677-7219A>T
ENST00000317502.10:c.753-7219A>T ENSP00000323047.6:n.753-7219A>T
ENST00000432508.3:c.600-7219A>T ENSP00000393480.2:n.600-7219A>T
ENST00000460848.5:n.1336-7219A>T
ENST00000468317.2:c.768-7219A>T ENSP00000436767.1:n.768-7219A>T
ENST00000473735.1:n.1607-7219A>T
ENST00000477902.6:c.630-7219A>T ENSP00000475596.1:n.630-7219A>T
NM_138384.2:c.753-7219A>T NP_612393.2:n.753-7219A>T
NM_138384.3:c.753-7219A>T NP_612393.2:n.753-7219A>T
NM_138384.4:c.753-7219A>T MANE Select NP_612393.2:n.753-7219A>T