Canonical Allele Identifier: CA340171577

Gene: POMGNT1 TSPAN1

Linked Data

• MyVariant Identifiers: chr1:g.46655637G>C (hg19) ; chr1:g.46189965G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46189965G>C , CM000663.2:g.46189965G>C	GRCh38
NC_000001.10:g.46655637G>C , CM000663.1:g.46655637G>C	GRCh37
NC_000001.9:g.46428224G>C	NCBI36
NG_009205.2:g.35341C>G
NG_009205.3:g.35341C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396420.8:c.1674C>G (POMGNT1)	ENSP00000379698.4:p.Ser558Arg
ENST00000497439.6:n.1846C>G (POMGNT1)
ENST00000684817.1:n.2034C>G (POMGNT1)
ENST00000684898.1:n.2236C>G (POMGNT1)
ENST00000685230.1:c.*984C>G (POMGNT1)	ENSP00000510305.1:n.*984C>G
ENST00000685275.1:n.2221C>G (POMGNT1)
ENST00000685444.1:c.1575C>G (POMGNT1)	ENSP00000510762.1:p.Ser525Arg
ENST00000685704.1:n.2340C>G (POMGNT1)
ENST00000685833.1:n.4067C>G (POMGNT1)
ENST00000686252.1:n.2748C>G (POMGNT1)
ENST00000686379.1:c.*798C>G (POMGNT1)	ENSP00000508913.1:n.*798C>G
ENST00000686724.1:n.3361C>G (POMGNT1)
ENST00000686737.1:c.1674C>G (POMGNT1)	ENSP00000508736.1:p.Ser558Arg
ENST00000687112.1:n.2540C>G (POMGNT1)
ENST00000687149.1:c.1713C>G (POMGNT1)	ENSP00000509745.1:p.Ser571Arg
ENST00000687197.1:c.*614C>G (POMGNT1)	ENSP00000510749.1:n.*614C>G
ENST00000687235.1:n.3751C>G (POMGNT1)
ENST00000687613.1:n.2314C>G (POMGNT1)
ENST00000687683.1:c.1674C>G (POMGNT1)	ENSP00000508522.1:p.Ser558Arg
ENST00000688032.1:n.2211C>G (POMGNT1)
ENST00000688596.1:n.2325C>G (POMGNT1)
ENST00000688608.1:c.1575C>G (POMGNT1)	ENSP00000508890.1:p.Ser525Arg
ENST00000689031.1:n.2126C>G (POMGNT1)
ENST00000689756.1:c.*1306C>G (POMGNT1)	ENSP00000509023.1:n.*1306C>G
ENST00000690377.1:n.2021C>G (POMGNT1)
ENST00000690678.1:c.1674C>G (POMGNT1)	ENSP00000508703.1:p.Ser558Arg
ENST00000691209.1:c.*614C>G (POMGNT1)	ENSP00000510112.1:n.*614C>G
ENST00000691243.1:c.*65C>G (POMGNT1)	ENSP00000510654.1:n.*65C>G
ENST00000692202.1:n.2249C>G (POMGNT1)
ENST00000692322.1:c.*1461C>G (POMGNT1)	ENSP00000509017.1:n.*1461C>G
ENST00000692369.1:c.1674C>G (POMGNT1)	ENSP00000508453.1:p.Ser558Arg
ENST00000692599.1:n.3549C>G (POMGNT1)
ENST00000692635.1:c.*549C>G (POMGNT1)	ENSP00000508425.1:n.*549C>G
ENST00000693168.1:n.3450C>G (POMGNT1)
ENST00000693218.1:c.*235C>G (POMGNT1)	ENSP00000510577.1:n.*235C>G
ENST00000693223.1:n.2622C>G (POMGNT1)
ENST00000371984.8:c.1674C>G (POMGNT1) MANE Select	ENSP00000361052.3:p.Ser558Arg
ENST00000371984.7:c.1674C>G (POMGNT1)	ENSP00000361052.3:p.Ser558Arg
ENST00000371992.1:c.1674C>G (POMGNT1)	ENSP00000361060.1:p.Ser558Arg
ENST00000396420.7:c.*1343C>G (POMGNT1)	ENSP00000379698.3:n.*1343C>G
ENST00000480972.1:n.323C>G (POMGNT1)
NM_001243766.1:c.1674C>G (POMGNT1)	NP_001230695.1:p.Ser558Arg
NM_001290129.1:c.1608C>G (POMGNT1)	NP_001277058.1:p.Ser536Arg
NM_001290130.1:c.1245C>G (POMGNT1)	NP_001277059.1:p.Ser415Arg
NM_017739.3:c.1674C>G (POMGNT1)	NP_060209.3:p.Ser558Arg
XM_005271010.1:c.1674C>G (POMGNT1)	XP_005271067.1:p.Ser558Arg
XM_006710755.1:c.1674C>G (POMGNT1)	XP_006710818.1:p.Ser558Arg
XM_006710756.1:c.1674C>G (POMGNT1)	XP_006710819.1:p.Ser558Arg
XM_011540460.1:c.678+4657G>C (TSPAN1)	XP_011538762.1:n.678+4657G>C
XM_011540461.1:c.633+4657G>C (TSPAN1)	XP_011538763.1:n.633+4657G>C
XM_011541759.1:c.1608C>G (POMGNT1)	XP_011540061.1:p.Ser536Arg
XM_011541760.1:c.1608C>G (POMGNT1)	XP_011540062.1:p.Ser536Arg
XM_011541761.1:c.582C>G (POMGNT1)	XP_011540063.1:p.Ser194Arg
XM_011540460.3:c.678+4657G>C (TSPAN1)	XP_011538762.1:n.678+4657G>C
XM_011541760.3:c.1608C>G (POMGNT1)	XP_011540062.1:p.Ser536Arg
XM_017001690.1:c.1674C>G (POMGNT1)	XP_016857179.1:p.Ser558Arg
NM_001243766.2:c.1674C>G (POMGNT1)	NP_001230695.2:p.Ser558Arg
NM_001290129.2:c.1608C>G (POMGNT1)	NP_001277058.2:p.Ser536Arg
NM_001290130.2:c.1245C>G (POMGNT1)	NP_001277059.2:p.Ser415Arg
NM_017739.4:c.1674C>G (POMGNT1) MANE Select	NP_060209.4:p.Ser558Arg