Canonical Allele Identifier: CA417886191

Gene: POMGNT1 TSPAN1

Linked Data

• MyVariant Identifiers: chr1:g.46657980C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46192308C>T , CM000663.2:g.46192308C>T	GRCh38
NC_000001.10:g.46657980C>T , CM000663.1:g.46657980C>T	GRCh37
NC_000001.9:g.46430567C>T	NCBI36
NG_009205.2:g.32998G>A
NG_009205.3:g.32998G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396420.8:c.1413G>A (POMGNT1)	ENSP00000379698.4:p.Lys471=
ENST00000477114.2:n.1975G>A (POMGNT1)
ENST00000497439.6:n.1585G>A (POMGNT1)
ENST00000684817.1:n.1773G>A (POMGNT1)
ENST00000684898.1:n.1975G>A (POMGNT1)
ENST00000685230.1:c.*723G>A (POMGNT1)	ENSP00000510305.1:n.*723G>A
ENST00000685275.1:n.1960G>A (POMGNT1)
ENST00000685444.1:c.1314G>A (POMGNT1)	ENSP00000510762.1:p.Lys438=
ENST00000685704.1:n.1975G>A (POMGNT1)
ENST00000685775.1:n.2940G>A (POMGNT1)
ENST00000685833.1:n.2291G>A (POMGNT1)
ENST00000686252.1:n.2487G>A (POMGNT1)
ENST00000686379.1:c.*537G>A (POMGNT1)	ENSP00000508913.1:n.*537G>A
ENST00000686724.1:n.1585G>A (POMGNT1)
ENST00000686737.1:c.1413G>A (POMGNT1)	ENSP00000508736.1:p.Lys471=
ENST00000687112.1:n.2279G>A (POMGNT1)
ENST00000687149.1:c.1413G>A (POMGNT1)	ENSP00000509745.1:p.Lys471=
ENST00000687197.1:c.*353G>A (POMGNT1)	ENSP00000510749.1:n.*353G>A
ENST00000687235.1:n.1975G>A (POMGNT1)
ENST00000687613.1:n.2163G>A (POMGNT1)
ENST00000687683.1:c.1413G>A (POMGNT1)	ENSP00000508522.1:p.Lys471=
ENST00000688032.1:n.1975G>A (POMGNT1)
ENST00000688596.1:n.2064G>A (POMGNT1)
ENST00000688608.1:c.1314G>A (POMGNT1)	ENSP00000508890.1:p.Lys438=
ENST00000688919.1:n.2609G>A (POMGNT1)
ENST00000689031.1:n.1975G>A (POMGNT1)
ENST00000689717.1:n.1585G>A (POMGNT1)
ENST00000689756.1:c.*1045G>A (POMGNT1)	ENSP00000509023.1:n.*1045G>A
ENST00000690377.1:n.1760G>A (POMGNT1)
ENST00000690678.1:c.1413G>A (POMGNT1)	ENSP00000508703.1:p.Lys471=
ENST00000691209.1:c.*353G>A (POMGNT1)	ENSP00000510112.1:n.*353G>A
ENST00000691243.1:c.1413G>A (POMGNT1)	ENSP00000510654.1:p.Lys471=
ENST00000692169.1:n.1562G>A (POMGNT1)
ENST00000692202.1:n.1988G>A (POMGNT1)
ENST00000692322.1:c.*1265G>A (POMGNT1)	ENSP00000509017.1:n.*1265G>A
ENST00000692369.1:c.1413G>A (POMGNT1)	ENSP00000508453.1:p.Lys471=
ENST00000692599.1:n.1975G>A (POMGNT1)
ENST00000692635.1:c.*353G>A (POMGNT1)	ENSP00000508425.1:n.*353G>A
ENST00000693168.1:n.1674G>A (POMGNT1)
ENST00000693218.1:c.1413G>A (POMGNT1)	ENSP00000510577.1:p.Lys471=
ENST00000693223.1:n.2361G>A (POMGNT1)
ENST00000693365.1:n.4047G>A (POMGNT1)
ENST00000371984.8:c.1413G>A (POMGNT1) MANE Select	ENSP00000361052.3:p.Lys471=
ENST00000371984.7:c.1413G>A (POMGNT1)	ENSP00000361052.3:p.Lys471=
ENST00000371992.1:c.1413G>A (POMGNT1)	ENSP00000361060.1:p.Lys471=
ENST00000396420.7:c.*1082G>A (POMGNT1)	ENSP00000379698.3:n.*1082G>A
ENST00000463030.1:n.34G>A (POMGNT1)
ENST00000485714.1:n.799G>A (POMGNT1)
NM_001243766.1:c.1413G>A (POMGNT1)	NP_001230695.1:p.Lys471=
NM_001290129.1:c.1347G>A (POMGNT1)	NP_001277058.1:p.Lys449=
NM_001290130.1:c.984G>A (POMGNT1)	NP_001277059.1:p.Lys328=
NM_017739.3:c.1413G>A (POMGNT1)	NP_060209.3:p.Lys471=
XM_005271010.1:c.1413G>A (POMGNT1)	XP_005271067.1:p.Lys471=
XM_006710755.1:c.1413G>A (POMGNT1)	XP_006710818.1:p.Lys471=
XM_006710756.1:c.1413G>A (POMGNT1)	XP_006710819.1:p.Lys471=
XM_011540460.1:c.679-3894C>T (TSPAN1)	XP_011538762.1:n.679-3894C>T
XM_011540461.1:c.634-3894C>T (TSPAN1)	XP_011538763.1:n.634-3894C>T
XM_011541759.1:c.1347G>A (POMGNT1)	XP_011540061.1:p.Lys449=
XM_011541760.1:c.1347G>A (POMGNT1)	XP_011540062.1:p.Lys449=
XM_011541761.1:c.321G>A (POMGNT1)	XP_011540063.1:p.Lys107=
XR_946706.1:n.1573G>A (POMGNT1)
XM_011540460.3:c.679-3894C>T (TSPAN1)	XP_011538762.1:n.679-3894C>T
XM_011541760.3:c.1347G>A (POMGNT1)	XP_011540062.1:p.Lys449=
XM_017001690.1:c.1413G>A (POMGNT1)	XP_016857179.1:p.Lys471=
NM_001243766.2:c.1413G>A (POMGNT1)	NP_001230695.2:p.Lys471=
NM_001290129.2:c.1347G>A (POMGNT1)	NP_001277058.2:p.Lys449=
NM_001290130.2:c.984G>A (POMGNT1)	NP_001277059.2:p.Lys328=
NM_017739.4:c.1413G>A (POMGNT1) MANE Select	NP_060209.4:p.Lys471=