Canonical Allele Identifier: CA340175899

Gene: POMGNT1 TSPAN1

Linked Data

• MyVariant Identifiers: chr1:g.46658095G>T (hg19) ; chr1:g.46192423G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46192423G>T , CM000663.2:g.46192423G>T	GRCh38
NC_000001.10:g.46658095G>T , CM000663.1:g.46658095G>T	GRCh37
NC_000001.9:g.46430682G>T	NCBI36
NG_009205.2:g.32883C>A
NG_009205.3:g.32883C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396420.8:c.1298C>A (POMGNT1)	ENSP00000379698.4:p.Thr433Lys
ENST00000477114.2:n.1860C>A (POMGNT1)
ENST00000497439.6:n.1470C>A (POMGNT1)
ENST00000684817.1:n.1658C>A (POMGNT1)
ENST00000684898.1:n.1860C>A (POMGNT1)
ENST00000685230.1:c.*608C>A (POMGNT1)	ENSP00000510305.1:n.*608C>A
ENST00000685275.1:n.1845C>A (POMGNT1)
ENST00000685444.1:c.1199C>A (POMGNT1)	ENSP00000510762.1:p.Thr400Lys
ENST00000685704.1:n.1860C>A (POMGNT1)
ENST00000685775.1:n.2825C>A (POMGNT1)
ENST00000685833.1:n.2176C>A (POMGNT1)
ENST00000686252.1:n.2372C>A (POMGNT1)
ENST00000686379.1:c.*422C>A (POMGNT1)	ENSP00000508913.1:n.*422C>A
ENST00000686724.1:n.1470C>A (POMGNT1)
ENST00000686737.1:c.1298C>A (POMGNT1)	ENSP00000508736.1:p.Thr433Lys
ENST00000687112.1:n.2164C>A (POMGNT1)
ENST00000687149.1:c.1298C>A (POMGNT1)	ENSP00000509745.1:p.Thr433Lys
ENST00000687197.1:c.*238C>A (POMGNT1)	ENSP00000510749.1:n.*238C>A
ENST00000687235.1:n.1860C>A (POMGNT1)
ENST00000687613.1:n.2048C>A (POMGNT1)
ENST00000687683.1:c.1298C>A (POMGNT1)	ENSP00000508522.1:p.Thr433Lys
ENST00000688032.1:n.1860C>A (POMGNT1)
ENST00000688596.1:n.1949C>A (POMGNT1)
ENST00000688608.1:c.1199C>A (POMGNT1)	ENSP00000508890.1:p.Thr400Lys
ENST00000688919.1:n.2494C>A (POMGNT1)
ENST00000689031.1:n.1860C>A (POMGNT1)
ENST00000689717.1:n.1470C>A (POMGNT1)
ENST00000689756.1:c.*930C>A (POMGNT1)	ENSP00000509023.1:n.*930C>A
ENST00000690377.1:n.1645C>A (POMGNT1)
ENST00000690678.1:c.1298C>A (POMGNT1)	ENSP00000508703.1:p.Thr433Lys
ENST00000691209.1:c.*238C>A (POMGNT1)	ENSP00000510112.1:n.*238C>A
ENST00000691243.1:c.1298C>A (POMGNT1)	ENSP00000510654.1:p.Thr433Lys
ENST00000692169.1:n.1447C>A (POMGNT1)
ENST00000692202.1:n.1873C>A (POMGNT1)
ENST00000692322.1:c.*1150C>A (POMGNT1)	ENSP00000509017.1:n.*1150C>A
ENST00000692369.1:c.1298C>A (POMGNT1)	ENSP00000508453.1:p.Thr433Lys
ENST00000692599.1:n.1860C>A (POMGNT1)
ENST00000692635.1:c.*238C>A (POMGNT1)	ENSP00000508425.1:n.*238C>A
ENST00000693168.1:n.1559C>A (POMGNT1)
ENST00000693218.1:c.1298C>A (POMGNT1)	ENSP00000510577.1:p.Thr433Lys
ENST00000693223.1:n.2246C>A (POMGNT1)
ENST00000693365.1:n.3932C>A (POMGNT1)
ENST00000371984.8:c.1298C>A (POMGNT1) MANE Select	ENSP00000361052.3:p.Thr433Lys
ENST00000371984.7:c.1298C>A (POMGNT1)	ENSP00000361052.3:p.Thr433Lys
ENST00000371992.1:c.1298C>A (POMGNT1)	ENSP00000361060.1:p.Thr433Lys
ENST00000396420.7:c.*967C>A (POMGNT1)	ENSP00000379698.3:n.*967C>A
ENST00000485714.1:n.684C>A (POMGNT1)
NM_001243766.1:c.1298C>A (POMGNT1)	NP_001230695.1:p.Thr433Lys
NM_001290129.1:c.1232C>A (POMGNT1)	NP_001277058.1:p.Thr411Lys
NM_001290130.1:c.869C>A (POMGNT1)	NP_001277059.1:p.Thr290Lys
NM_017739.3:c.1298C>A (POMGNT1)	NP_060209.3:p.Thr433Lys
XM_005271010.1:c.1298C>A (POMGNT1)	XP_005271067.1:p.Thr433Lys
XM_006710755.1:c.1298C>A (POMGNT1)	XP_006710818.1:p.Thr433Lys
XM_006710756.1:c.1298C>A (POMGNT1)	XP_006710819.1:p.Thr433Lys
XM_011540460.1:c.679-3779G>T (TSPAN1)	XP_011538762.1:n.679-3779G>T
XM_011540461.1:c.634-3779G>T (TSPAN1)	XP_011538763.1:n.634-3779G>T
XM_011541759.1:c.1232C>A (POMGNT1)	XP_011540061.1:p.Thr411Lys
XM_011541760.1:c.1232C>A (POMGNT1)	XP_011540062.1:p.Thr411Lys
XM_011541761.1:c.206C>A (POMGNT1)	XP_011540063.1:p.Thr69Lys
XR_946706.1:n.1458C>A (POMGNT1)
XM_011540460.3:c.679-3779G>T (TSPAN1)	XP_011538762.1:n.679-3779G>T
XM_011541760.3:c.1232C>A (POMGNT1)	XP_011540062.1:p.Thr411Lys
XM_017001690.1:c.1298C>A (POMGNT1)	XP_016857179.1:p.Thr433Lys
NM_001243766.2:c.1298C>A (POMGNT1)	NP_001230695.2:p.Thr433Lys
NM_001290129.2:c.1232C>A (POMGNT1)	NP_001277058.2:p.Thr411Lys
NM_001290130.2:c.869C>A (POMGNT1)	NP_001277059.2:p.Thr290Lys
NM_017739.4:c.1298C>A (POMGNT1) MANE Select	NP_060209.4:p.Thr433Lys