Canonical Allele Identifier: CA2830538759

Gene: TMEM171

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.73131797_73131798insT , CM000667.2:g.73131797_73131798insT	GRCh38
NC_000005.9:g.72427624_72427625insT , CM000667.1:g.72427624_72427625insT	GRCh37
NC_000005.8:g.72463380_72463381insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454765.7:c.*67_*68insT MANE Select	ENSP00000415030.2:n.*67_*68insT
ENST00000287773.5:c.*67_*68insT	ENSP00000287773.5:n.*67_*68insT
ENST00000454765.6:c.*67_*68insT	ENSP00000415030.2:n.*67_*68insT
NM_001161342.2:c.*67_*68insT	NP_001154814.1:n.*67_*68insT
NM_173490.7:c.*67_*68insT	NP_775761.4:n.*67_*68insT
XM_011543156.1:c.*67_*68insT	XP_011541458.1:n.*67_*68insT
NM_173490.8:c.*67_*68insT MANE Select	NP_775761.4:n.*67_*68insT
NM_001161342.3:c.*67_*68insT	NP_001154814.1:n.*67_*68insT