Canonical Allele Identifier: CA2148342306

Gene: POMT2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77301100C= , CM000676.2:g.77301100C=	GRCh38
NC_000014.8:g.77767443C= , CM000676.1:g.77767443C=	GRCh37
NC_000014.7:g.76837196C=	NCBI36
NG_008897.1:g.24783G= , LRG_844:g.24783G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553863.6:c.259G=	ENSP00000508202.1:n.259G=
ENST00000556394.2:c.358-1539G=	ENSP00000451967.2:n.358-1539G=
ENST00000557289.2:c.150G=
ENST00000682247.1:c.806G=	ENSP00000507213.1:p.Ser269=
ENST00000682382.1:c.496-2329G=
ENST00000682395.1:n.535G=
ENST00000682459.1:n.470G=
ENST00000682467.1:c.806G=	ENSP00000508062.1:p.Ser269=
ENST00000682795.1:c.806G=	ENSP00000507574.1:p.Ser269=
ENST00000682895.1:n.522G=
ENST00000682955.1:n.212-2329G=
ENST00000683167.1:c.150G=
ENST00000683188.1:c.343-1539G=
ENST00000683300.1:c.109+3592G=	ENSP00000507630.1:n.109+3592G=
ENST00000683328.1:c.109+3592G=	ENSP00000508096.1:n.109+3592G=
ENST00000683380.1:n.470G=
ENST00000683398.1:c.150G=
ENST00000683551.1:c.109+1735G=
ENST00000683828.1:c.526-1539G=
ENST00000684259.1:n.657G=
ENST00000684549.1:n.368-1539G=
ENST00000684554.1:c.150G=
ENST00000261534.9:c.806G= MANE Select	ENSP00000261534.4:p.Ser269=
ENST00000261534.8:c.806G=	ENSP00000261534.4:p.Ser269=
ENST00000452340.7:n.829G=
ENST00000553863.5:n.470G=
ENST00000554767.5:n.64G=
ENST00000555675.5:n.522G=
ENST00000556326.5:c.*472G=	ENSP00000450630.1:n.*472G=
ENST00000557289.1:c.56-1539G=	ENSP00000451115.1:n.56-1539G=
NM_013382.5:c.806G= , LRG_844t1:c.806G=	NP_037514.2:p.Ser269=
XM_011536675.1:c.806G=	XP_011534977.1:p.Ser269=
XM_011536676.1:c.473G=	XP_011534978.1:p.Ser158=
XM_011536677.1:c.547+3592G=	XP_011534979.1:n.547+3592G=
XM_011536678.1:c.806G=	XP_011534980.1:p.Ser269=
XM_011536679.1:c.-90-1539G=	XP_011534981.1:n.-90-1539G=
XM_011536680.1:c.806G=	XP_011534982.1:p.Ser269=
XR_943416.1:n.1009G=
XM_011536675.2:c.806G=	XP_011534977.1:p.Ser269=
XM_011536676.2:c.473G=	XP_011534978.1:p.Ser158=
XM_011536677.3:c.547+3592G=	XP_011534979.1:n.547+3592G=
XR_001750279.1:n.1006G=
XR_001750282.1:n.1010G=
XR_943416.3:n.1007G=
NM_013382.6:c.806G=	NP_037514.2:p.Ser269=
NM_013382.7:c.806G= MANE Select	NP_037514.2:p.Ser269=