Canonical Allele Identifier: CA1621689396

Gene: TMEM217B TMEM217

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37212763G= , CM000668.2:g.37212763G=	GRCh38
NC_000006.11:g.37180539G= , CM000668.1:g.37180539G=	GRCh37
NC_000006.10:g.37288517G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000497775.2:c.207C= (TMEM217B) MANE Select	ENSP00000499172.1:p.Ile69=
ENST00000651039.2:c.*203C= (TMEM217) MANE Select	ENSP00000499204.1:n.*203C=
ENST00000336655.7:c.*234C= (TMEM217)	ENSP00000338164.2:n.*234C=
ENST00000356757.7:c.*203C= (TMEM217)	ENSP00000349198.2:n.*203C=
ENST00000478262.2:c.207C= (TMEM217B)	ENSP00000498233.1:p.Ile69=
ENST00000650809.1:c.*333C= (TMEM217)	ENSP00000498285.1:n.*333C=
ENST00000650812.1:c.207C= (TMEM217B)	ENSP00000498349.1:p.Ile69=
ENST00000650973.1:c.*343C= (TMEM217)	ENSP00000498793.1:n.*343C=
ENST00000651039.1:c.*203C= (TMEM217)	ENSP00000499204.1:n.*203C=
ENST00000651722.1:c.531C= (TMEM217)
ENST00000652218.1:c.*208C= (TMEM217)	ENSP00000498862.1:n.*208C=
ENST00000652386.1:c.*203C= (TMEM217)	ENSP00000498681.1:n.*203C=
ENST00000652495.1:c.*128C= (TMEM217)	ENSP00000499097.1:n.*128C=
ENST00000336655.6:c.*234C= (TMEM217)	ENSP00000338164.2:n.*234C=
ENST00000356757.6:c.*203C= (TMEM217)	ENSP00000349198.2:n.*203C=
ENST00000478262.1:n.389C= (TMEM217)
ENST00000497775.1:n.303C= (TMEM217)
NM_001286401.1:c.*203C= (TMEM217)	NP_001273330.1:n.*203C=
NM_145316.3:c.*234C= (TMEM217)	NP_660359.2:n.*234C=
NR_104442.1:n.907C= (TMEM217)
NR_104443.1:n.822C= (TMEM217)
XM_011514368.1:c.207C= (TMEM217)	XP_011512670.1:p.Ile69=
XM_011514369.1:c.207C= (TMEM217)	XP_011512671.1:p.Ile69=
XM_011514370.1:c.207C= (TMEM217)	XP_011512672.1:p.Ile69=
XM_011514367.2:c.*208C= (TMEM217)	XP_011512669.1:n.*208C=
XM_011514369.3:c.207C= (TMEM217)	XP_011512671.1:p.Ile69=
XM_011514370.2:c.207C= (TMEM217)	XP_011512672.1:p.Ile69=
XM_024446353.1:c.*203C= (TMEM217)	XP_024302121.1:n.*203C=
NM_145316.4:c.*234C= (TMEM217)	NP_660359.2:n.*234C=
NM_001371555.1:c.*203C= (TMEM217)	NP_001358484.1:n.*203C=
NM_001286401.2:c.*203C= (TMEM217) MANE Select	NP_001273330.1:n.*203C=
NR_104442.2:n.896C= (TMEM217)
NR_104443.2:n.811C= (TMEM217)
NM_001395238.1:c.*208C= (TMEM217)	NP_001382167.1:n.*208C=
NM_001395241.1:c.*219C= (TMEM217)	NP_001382170.1:n.*219C=
NM_001395242.1:c.*219C= (TMEM217)	NP_001382171.1:n.*219C=
NM_001395243.1:c.*208C= (TMEM217)	NP_001382172.1:n.*208C=
NM_001395244.1:c.*128C= (TMEM217)	NP_001382173.1:n.*128C=
NM_001395377.1:c.207C= (TMEM217B)	NP_001382306.1:p.Ile69=
NM_001395378.1:c.207C= (TMEM217B) MANE Select	NP_001382307.1:p.Ile69=
NM_001395938.1:c.207C= (TMEM217B)	NP_001382867.1:p.Ile69=
NR_172517.1:n.1536C= (TMEM217)