Canonical Allele Identifier: CA391203026
Gene: TMEM121 HGNC NCBI

Linked Data

dbSNP Id: rs1555444290

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105529535C>T , CM000676.2:g.105529535C>T GRCh38
NC_000014.8:g.105995872C>T , CM000676.1:g.105995872C>T GRCh37
NC_000014.7:g.105066917C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392519.7:c.701C>T MANE Select ENSP00000376304.2:p.Ala234Val
ENST00000392519.6:c.701C>T ENSP00000376304.2:p.Ala234Val
ENST00000431372.1:c.701C>T ENSP00000407456.1:p.Ala234Val
NM_025268.2:c.701C>T NP_079544.1:p.Ala234Val
XM_005268101.2:c.701C>T XP_005268158.1:p.Ala234Val
XM_006720261.2:c.701C>T XP_006720324.1:p.Ala234Val
XM_011537185.1:c.701C>T XP_011535487.1:p.Ala234Val
XM_011537186.1:c.701C>T XP_011535488.1:p.Ala234Val
NM_001331238.1:c.701C>T NP_001318167.1:p.Ala234Val
NM_025268.3:c.701C>T NP_079544.1:p.Ala234Val
XM_006720261.3:c.701C>T XP_006720324.1:p.Ala234Val
NM_025268.4:c.701C>T MANE Select NP_079544.1:p.Ala234Val
NM_001331238.2:c.701C>T NP_001318167.1:p.Ala234Val