Canonical Allele Identifier: CA735499766
Gene: MTF1 HGNC NCBI

Linked Data

dbSNP Id: rs1340419045
gnomAD v3: 1-37812701-TC-T
gnomAD v4: 1-37812701-TC-T
MyVariant Identifiers: chr1:g.38278374del (hg19) chr1:g.37812702del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.37812704del , CM000663.2:g.37812704del GRCh38
NC_000001.10:g.38278376del , CM000663.1:g.38278376del GRCh37
NC_000001.9:g.38050963del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000373036.5:c.*2434del MANE Select ENSP00000362127.3:n.*2434del
ENST00000373036.4:c.*2434del ENSP00000362127.3:n.*2434del
NM_005955.2:c.*2434del NP_005946.2:n.*2434del
XM_011541491.1:c.*2434del XP_011539793.1:n.*2434del
XM_011541492.1:c.*2434del XP_011539794.1:n.*2434del
XM_011541494.1:c.*2434del XP_011539796.1:n.*2434del
XM_011541491.2:c.*2434del XP_011539793.1:n.*2434del
NM_005955.3:c.*2434del MANE Select NP_005946.2:n.*2434del
Search 100 bp 5'
Search 100 bp 3'