Canonical Allele Identifier: CA934184939
Gene: MTG1 HGNC NCBI

Linked Data

dbSNP Id: rs1850057471

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133412206G>C , CM000672.2:g.133412206G>C GRCh38
NC_000010.10:g.135225710G>C , CM000672.1:g.135225710G>C GRCh37
NC_000010.9:g.135075700G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000317502.11:c.753-7274G>C MANE Select ENSP00000323047.6:n.753-7274G>C
ENST00000468317.3:c.*677-7274G>C ENSP00000436767.2:n.*677-7274G>C
ENST00000317502.10:c.753-7274G>C ENSP00000323047.6:n.753-7274G>C
ENST00000432508.3:c.600-7274G>C ENSP00000393480.2:n.600-7274G>C
ENST00000460848.5:n.1336-7274G>C
ENST00000468317.2:c.768-7274G>C ENSP00000436767.1:n.768-7274G>C
ENST00000473735.1:n.1607-7274G>C
ENST00000477902.6:c.630-7274G>C ENSP00000475596.1:n.630-7274G>C
NM_138384.2:c.753-7274G>C NP_612393.2:n.753-7274G>C
NM_138384.3:c.753-7274G>C NP_612393.2:n.753-7274G>C
NM_138384.4:c.753-7274G>C MANE Select NP_612393.2:n.753-7274G>C