Canonical Allele Identifier: CA2161352941

Gene: TMEM121

Linked Data

• dbSNP Id: rs2084629097

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105529818_105529825del , CM000676.2:g.105529818_105529825del	GRCh38
NC_000014.8:g.105996155_105996162del , CM000676.1:g.105996155_105996162del	GRCh37
NC_000014.7:g.105067200_105067207del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392519.7:c.*24_*31del MANE Select	ENSP00000376304.2:n.*24_*31del
ENST00000392519.6:c.*24_*31del	ENSP00000376304.2:n.*24_*31del
ENST00000431372.1:c.*24_*31del	ENSP00000407456.1:n.*24_*31del
NM_025268.2:c.*24_*31del	NP_079544.1:n.*24_*31del
XM_005268101.2:c.*24_*31del	XP_005268158.1:n.*24_*31del
XM_006720261.2:c.*24_*31del	XP_006720324.1:n.*24_*31del
XM_011537185.1:c.*24_*31del	XP_011535487.1:n.*24_*31del
XM_011537186.1:c.*24_*31del	XP_011535488.1:n.*24_*31del
NM_001331238.1:c.*24_*31del	NP_001318167.1:n.*24_*31del
NM_025268.3:c.*24_*31del	NP_079544.1:n.*24_*31del
XM_006720261.3:c.*24_*31del	XP_006720324.1:n.*24_*31del
NM_025268.4:c.*24_*31del MANE Select	NP_079544.1:n.*24_*31del
NM_001331238.2:c.*24_*31del	NP_001318167.1:n.*24_*31del