Canonical Allele Identifier: CA2678535601

Gene: TMEM217B TMEM217

Linked Data

• gnomAD v4: 6-37212758-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37212758C>T , CM000668.2:g.37212758C>T	GRCh38
NC_000006.11:g.37180534C>T , CM000668.1:g.37180534C>T	GRCh37
NC_000006.10:g.37288512C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000497775.2:c.212G>A (TMEM217B) MANE Select	ENSP00000499172.1:p.Gly71Asp
ENST00000651039.2:c.*208G>A (TMEM217) MANE Select	ENSP00000499204.1:n.*208G>A
ENST00000336655.7:c.*239G>A (TMEM217)	ENSP00000338164.2:n.*239G>A
ENST00000356757.7:c.*208G>A (TMEM217)	ENSP00000349198.2:n.*208G>A
ENST00000478262.2:c.212G>A (TMEM217B)	ENSP00000498233.1:p.Gly71Asp
ENST00000650809.1:c.*338G>A (TMEM217)	ENSP00000498285.1:n.*338G>A
ENST00000650812.1:c.212G>A (TMEM217B)	ENSP00000498349.1:p.Gly71Asp
ENST00000650973.1:c.*348G>A (TMEM217)	ENSP00000498793.1:n.*348G>A
ENST00000651039.1:c.*208G>A (TMEM217)	ENSP00000499204.1:n.*208G>A
ENST00000651722.1:c.536G>A (TMEM217)
ENST00000652218.1:c.*213G>A (TMEM217)	ENSP00000498862.1:n.*213G>A
ENST00000652386.1:c.*208G>A (TMEM217)	ENSP00000498681.1:n.*208G>A
ENST00000652495.1:c.*133G>A (TMEM217)	ENSP00000499097.1:n.*133G>A
ENST00000336655.6:c.*239G>A (TMEM217)	ENSP00000338164.2:n.*239G>A
ENST00000356757.6:c.*208G>A (TMEM217)	ENSP00000349198.2:n.*208G>A
ENST00000478262.1:n.394G>A (TMEM217)
ENST00000497775.1:n.308G>A (TMEM217)
NM_001286401.1:c.*208G>A (TMEM217)	NP_001273330.1:n.*208G>A
NM_145316.3:c.*239G>A (TMEM217)	NP_660359.2:n.*239G>A
NR_104442.1:n.912G>A (TMEM217)
NR_104443.1:n.827G>A (TMEM217)
XM_011514368.1:c.212G>A (TMEM217)	XP_011512670.1:p.Gly71Asp
XM_011514369.1:c.212G>A (TMEM217)	XP_011512671.1:p.Gly71Asp
XM_011514370.1:c.212G>A (TMEM217)	XP_011512672.1:p.Gly71Asp
XM_011514367.2:c.*213G>A (TMEM217)	XP_011512669.1:n.*213G>A
XM_011514369.3:c.212G>A (TMEM217)	XP_011512671.1:p.Gly71Asp
XM_011514370.2:c.212G>A (TMEM217)	XP_011512672.1:p.Gly71Asp
XM_024446353.1:c.*208G>A (TMEM217)	XP_024302121.1:n.*208G>A
NM_145316.4:c.*239G>A (TMEM217)	NP_660359.2:n.*239G>A
NM_001371555.1:c.*208G>A (TMEM217)	NP_001358484.1:n.*208G>A
NM_001286401.2:c.*208G>A (TMEM217) MANE Select	NP_001273330.1:n.*208G>A
NR_104442.2:n.901G>A (TMEM217)
NR_104443.2:n.816G>A (TMEM217)
NM_001395238.1:c.*213G>A (TMEM217)	NP_001382167.1:n.*213G>A
NM_001395241.1:c.*224G>A (TMEM217)	NP_001382170.1:n.*224G>A
NM_001395242.1:c.*224G>A (TMEM217)	NP_001382171.1:n.*224G>A
NM_001395243.1:c.*213G>A (TMEM217)	NP_001382172.1:n.*213G>A
NM_001395244.1:c.*133G>A (TMEM217)	NP_001382173.1:n.*133G>A
NM_001395377.1:c.212G>A (TMEM217B)	NP_001382306.1:p.Gly71Asp
NM_001395378.1:c.212G>A (TMEM217B) MANE Select	NP_001382307.1:p.Gly71Asp
NM_001395938.1:c.212G>A (TMEM217B)	NP_001382867.1:p.Gly71Asp
NR_172517.1:n.1541G>A (TMEM217)