Canonical Allele Identifier: CA391203279
Gene: TMEM121 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105529652A>C , CM000676.2:g.105529652A>C GRCh38
NC_000014.8:g.105995989A>C , CM000676.1:g.105995989A>C GRCh37
NC_000014.7:g.105067034A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392519.7:c.818A>C MANE Select ENSP00000376304.2:p.Asp273Ala
ENST00000392519.6:c.818A>C ENSP00000376304.2:p.Asp273Ala
ENST00000431372.1:c.818A>C ENSP00000407456.1:p.Asp273Ala
NM_025268.2:c.818A>C NP_079544.1:p.Asp273Ala
XM_005268101.2:c.818A>C XP_005268158.1:p.Asp273Ala
XM_006720261.2:c.818A>C XP_006720324.1:p.Asp273Ala
XM_011537185.1:c.818A>C XP_011535487.1:p.Asp273Ala
XM_011537186.1:c.818A>C XP_011535488.1:p.Asp273Ala
NM_001331238.1:c.818A>C NP_001318167.1:p.Asp273Ala
NM_025268.3:c.818A>C NP_079544.1:p.Asp273Ala
XM_006720261.3:c.818A>C XP_006720324.1:p.Asp273Ala
NM_025268.4:c.818A>C MANE Select NP_079544.1:p.Asp273Ala
NM_001331238.2:c.818A>C NP_001318167.1:p.Asp273Ala