Canonical Allele Identifier: CA1163306521
Gene: MTF1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.37813131T= , CM000663.2:g.37813131T= GRCh38
NC_000001.10:g.38278803T= , CM000663.1:g.38278803T= GRCh37
NC_000001.9:g.38051390T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000373036.5:c.*2005A= MANE Select ENSP00000362127.3:n.*2005A=
ENST00000373036.4:c.*2005A= ENSP00000362127.3:n.*2005A=
NM_005955.2:c.*2005A= NP_005946.2:n.*2005A=
XM_011541491.1:c.*2005A= XP_011539793.1:n.*2005A=
XM_011541492.1:c.*2005A= XP_011539794.1:n.*2005A=
XM_011541494.1:c.*2005A= XP_011539796.1:n.*2005A=
XM_011541491.2:c.*2005A= XP_011539793.1:n.*2005A=
NM_005955.3:c.*2005A= MANE Select NP_005946.2:n.*2005A=
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