Canonical Allele Identifier: CA8911044

Gene: TMEM241

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23356649C>T , CM000680.2:g.23356649C>T	GRCh38
NC_000018.9:g.20936613C>T , CM000680.1:g.20936613C>T	GRCh37
NC_000018.8:g.19190611C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032933.6:c.616G>A MANE Select	NP_116322.3:p.Val206Ile
ENST00000383233.8:c.616G>A MANE Select	ENSP00000372720.3:p.Val206Ile
NM_001318834.1:c.253G>A	NP_001305763.1:p.Val85Ile
NM_001318834.2:c.253G>A	NP_001305763.1:p.Val85Ile
NM_032933.4:c.616G>A	NP_116322.3:p.Val206Ile
NM_032933.5:c.616G>A	NP_116322.3:p.Val206Ile
NR_134875.1:n.684G>A
NR_134875.2:n.676G>A
NR_134876.1:n.604G>A
NR_134876.2:n.596G>A
NR_134877.1:n.687G>A
NR_134877.2:n.679G>A
NR_148382.1:n.608G>A
NR_148382.2:n.600G>A
NR_148383.1:n.686G>A
NR_148383.2:n.678G>A
NR_148384.1:n.637G>A
NR_148384.2:n.629G>A
NR_148385.1:n.651G>A
NR_148385.2:n.643G>A
ENST00000383233.7:c.616G>A	ENSP00000372720.3:p.Val206Ile
ENST00000460322.5:c.*254G>A	ENSP00000433795.1:n.*254G>A
ENST00000473688.5:c.*87G>A	ENSP00000431584.1:n.*87G>A
ENST00000477053.5:c.*115G>A	ENSP00000437280.1:n.*115G>A
ENST00000482411.5:c.*259G>A	ENSP00000435139.1:n.*259G>A
ENST00000497608.5:c.*303G>A	ENSP00000433605.1:n.*303G>A
ENST00000542162.5:c.*281G>A	ENSP00000440152.2:n.*281G>A
ENST00000577531.5:c.571G>A	ENSP00000464008.1:n.571G>A
ENST00000578520.5:c.499G>A	ENSP00000464174.1:p.Val167Ile
ENST00000581444.5:c.*418G>A	ENSP00000462199.1:n.*418G>A
ENST00000583048.5:n.152G>A
XM_005258373.2:c.616G>A	XP_005258430.1:p.Val206Ile
XM_011526232.1:c.616G>A	XP_011524534.1:p.Val206Ile
XM_011526233.1:c.616G>A	XP_011524535.1:p.Val206Ile
XM_011526233.2:c.616G>A	XP_011524535.1:p.Val206Ile
XM_011526234.1:c.616G>A	XP_011524536.1:p.Val206Ile
XM_011526235.1:c.*51G>A	XP_011524537.1:n.*51G>A
XM_017026043.1:c.616G>A	XP_016881532.1:p.Val206Ile
XM_017026044.2:c.616G>A	XP_016881533.1:p.Val206Ile
XM_017026045.1:c.538G>A	XP_016881534.1:p.Val180Ile
XM_017026046.1:c.253G>A	XP_016881535.1:p.Val85Ile
XM_017026047.1:c.253G>A	XP_016881536.1:p.Val85Ile
XM_017026049.1:c.253G>A	XP_016881538.1:p.Val85Ile
XM_017026050.1:c.253G>A	XP_016881539.1:p.Val85Ile
XM_017026051.1:c.253G>A	XP_016881540.1:p.Val85Ile
XM_024451277.1:c.253G>A	XP_024307045.1:p.Val85Ile
XR_001753287.1:n.723G>A
XR_001753288.1:n.723G>A
XR_001753289.1:n.723G>A
XR_001753290.2:n.590G>A
XR_001753291.1:n.557G>A
XR_001753292.2:n.831G>A
XR_001753293.1:n.787G>A
XR_243852.2:n.723G>A
XR_243853.1:n.677G>A
XR_935258.1:n.557G>A
XR_935259.1:n.557G>A
XR_935260.1:n.557G>A