Canonical Allele Identifier: CA390520916

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77772684C>T (hg19) ; chr14:g.77306341C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306341C>T , CM000676.2:g.77306341C>T	GRCh38
NC_000014.8:g.77772684C>T , CM000676.1:g.77772684C>T	GRCh37
NC_000014.7:g.76842437C>T	NCBI36
NG_008897.1:g.19542G>A , LRG_844:g.19542G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555675.6:n.163G>A
ENST00000556394.2:c.249-1541G>A	ENSP00000451967.2:n.249-1541G>A
ENST00000556880.6:n.367G>A
ENST00000682247.1:c.434G>A	ENSP00000507213.1:p.Arg145Lys
ENST00000682382.1:c.382G>A
ENST00000682395.1:n.163G>A
ENST00000682459.1:n.102+61G>A
ENST00000682467.1:c.434G>A	ENSP00000508062.1:p.Arg145Lys
ENST00000682795.1:c.434G>A	ENSP00000507574.1:p.Arg145Lys
ENST00000682895.1:n.150G>A
ENST00000682955.1:n.102+61G>A
ENST00000683188.1:c.229G>A
ENST00000683380.1:n.102+61G>A
ENST00000683828.1:c.303G>A
ENST00000684066.1:n.129G>A
ENST00000684102.1:n.180G>A
ENST00000684259.1:n.285G>A
ENST00000684479.1:n.101G>A
ENST00000684549.1:n.163G>A
ENST00000684600.1:c.248G>A
ENST00000684670.1:n.101G>A
ENST00000684746.1:n.131G>A
ENST00000261534.9:c.434G>A MANE Select	ENSP00000261534.4:p.Arg145Lys
ENST00000261534.8:c.434G>A	ENSP00000261534.4:p.Arg145Lys
ENST00000452340.7:n.457G>A
ENST00000553863.5:n.102+61G>A
ENST00000554948.1:c.161G>A	ENSP00000452060.1:p.Arg54Lys
ENST00000555675.5:n.150G>A
ENST00000555788.5:n.268G>A
ENST00000556326.5:c.*100G>A	ENSP00000450630.1:n.*100G>A
ENST00000556880.5:n.367G>A
ENST00000557525.1:n.524G>A
NM_013382.5:c.434G>A , LRG_844t1:c.434G>A	NP_037514.2:p.Arg145Lys
XM_011536675.1:c.434G>A	XP_011534977.1:p.Arg145Lys
XM_011536676.1:c.101G>A	XP_011534978.1:p.Arg34Lys
XM_011536677.1:c.434G>A	XP_011534979.1:p.Arg145Lys
XM_011536678.1:c.434G>A	XP_011534980.1:p.Arg145Lys
XM_011536680.1:c.434G>A	XP_011534982.1:p.Arg145Lys
XR_943416.1:n.637G>A
XM_011536675.2:c.434G>A	XP_011534977.1:p.Arg145Lys
XM_011536676.2:c.101G>A	XP_011534978.1:p.Arg34Lys
XM_011536677.3:c.434G>A	XP_011534979.1:p.Arg145Lys
XR_001750279.1:n.634G>A
XR_001750282.1:n.638G>A
XR_943416.3:n.635G>A
NM_013382.6:c.434G>A	NP_037514.2:p.Arg145Lys
NM_013382.7:c.434G>A MANE Select	NP_037514.2:p.Arg145Lys