Canonical Allele Identifier: CA487325735

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77772689T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306346T>A , CM000676.2:g.77306346T>A	GRCh38
NC_000014.8:g.77772689T>A , CM000676.1:g.77772689T>A	GRCh37
NC_000014.7:g.76842442T>A	NCBI36
NG_008897.1:g.19537A>T , LRG_844:g.19537A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555675.6:n.158A>T
ENST00000556394.2:c.249-1546A>T	ENSP00000451967.2:n.249-1546A>T
ENST00000556880.6:n.362A>T
ENST00000682247.1:c.429A>T	ENSP00000507213.1:p.Gly143=
ENST00000682382.1:c.377A>T
ENST00000682395.1:n.158A>T
ENST00000682459.1:n.102+56A>T
ENST00000682467.1:c.429A>T	ENSP00000508062.1:p.Gly143=
ENST00000682795.1:c.429A>T	ENSP00000507574.1:p.Gly143=
ENST00000682895.1:n.145A>T
ENST00000682955.1:n.102+56A>T
ENST00000683188.1:c.224A>T
ENST00000683380.1:n.102+56A>T
ENST00000683828.1:c.298A>T
ENST00000684066.1:n.124A>T
ENST00000684102.1:n.175A>T
ENST00000684259.1:n.280A>T
ENST00000684479.1:n.96A>T
ENST00000684549.1:n.158A>T
ENST00000684600.1:c.243A>T
ENST00000684670.1:n.96A>T
ENST00000684746.1:n.126A>T
ENST00000261534.9:c.429A>T MANE Select	ENSP00000261534.4:p.Gly143=
ENST00000261534.8:c.429A>T	ENSP00000261534.4:p.Gly143=
ENST00000452340.7:n.452A>T
ENST00000553863.5:n.102+56A>T
ENST00000554948.1:c.156A>T	ENSP00000452060.1:p.Gly52=
ENST00000555675.5:n.145A>T
ENST00000555788.5:n.263A>T
ENST00000556326.5:c.*95A>T	ENSP00000450630.1:n.*95A>T
ENST00000556880.5:n.362A>T
ENST00000557525.1:n.519A>T
NM_013382.5:c.429A>T , LRG_844t1:c.429A>T	NP_037514.2:p.Gly143=
XM_011536675.1:c.429A>T	XP_011534977.1:p.Gly143=
XM_011536676.1:c.96A>T	XP_011534978.1:p.Gly32=
XM_011536677.1:c.429A>T	XP_011534979.1:p.Gly143=
XM_011536678.1:c.429A>T	XP_011534980.1:p.Gly143=
XM_011536680.1:c.429A>T	XP_011534982.1:p.Gly143=
XR_943416.1:n.632A>T
XM_011536675.2:c.429A>T	XP_011534977.1:p.Gly143=
XM_011536676.2:c.96A>T	XP_011534978.1:p.Gly32=
XM_011536677.3:c.429A>T	XP_011534979.1:p.Gly143=
XR_001750279.1:n.629A>T
XR_001750282.1:n.633A>T
XR_943416.3:n.630A>T
NM_013382.6:c.429A>T	NP_037514.2:p.Gly143=
NM_013382.7:c.429A>T MANE Select	NP_037514.2:p.Gly143=