Canonical Allele Identifier: CA2626947275

Gene: TMEM121

Linked Data

• gnomAD v4: 14-105529808-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.105529812_105529813del , CM000676.2:g.105529812_105529813del	GRCh38
NC_000014.8:g.105996149_105996150del , CM000676.1:g.105996149_105996150del	GRCh37
NC_000014.7:g.105067194_105067195del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392519.7:c.*18_*19del MANE Select	ENSP00000376304.2:n.*18_*19del
ENST00000392519.6:c.*18_*19del	ENSP00000376304.2:n.*18_*19del
ENST00000431372.1:c.*18_*19del	ENSP00000407456.1:n.*18_*19del
NM_025268.2:c.*18_*19del	NP_079544.1:n.*18_*19del
XM_005268101.2:c.*18_*19del	XP_005268158.1:n.*18_*19del
XM_006720261.2:c.*18_*19del	XP_006720324.1:n.*18_*19del
XM_011537185.1:c.*18_*19del	XP_011535487.1:n.*18_*19del
XM_011537186.1:c.*18_*19del	XP_011535488.1:n.*18_*19del
NM_001331238.1:c.*18_*19del	NP_001318167.1:n.*18_*19del
NM_025268.3:c.*18_*19del	NP_079544.1:n.*18_*19del
XM_006720261.3:c.*18_*19del	XP_006720324.1:n.*18_*19del
NM_025268.4:c.*18_*19del MANE Select	NP_079544.1:n.*18_*19del
NM_001331238.2:c.*18_*19del	NP_001318167.1:n.*18_*19del