Canonical Allele Identifier: CA390520914

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77772683T>G (hg19) ; chr14:g.77306340T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306340T>G , CM000676.2:g.77306340T>G	GRCh38
NC_000014.8:g.77772683T>G , CM000676.1:g.77772683T>G	GRCh37
NC_000014.7:g.76842436T>G	NCBI36
NG_008897.1:g.19543A>C , LRG_844:g.19543A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555675.6:n.164A>C
ENST00000556394.2:c.249-1540A>C	ENSP00000451967.2:n.249-1540A>C
ENST00000556880.6:n.368A>C
ENST00000682247.1:c.435A>C	ENSP00000507213.1:p.Arg145Ser
ENST00000682382.1:c.383A>C
ENST00000682395.1:n.164A>C
ENST00000682459.1:n.102+62A>C
ENST00000682467.1:c.435A>C	ENSP00000508062.1:p.Arg145Ser
ENST00000682795.1:c.435A>C	ENSP00000507574.1:p.Arg145Ser
ENST00000682895.1:n.151A>C
ENST00000682955.1:n.102+62A>C
ENST00000683188.1:c.230A>C
ENST00000683380.1:n.102+62A>C
ENST00000683828.1:c.304A>C
ENST00000684066.1:n.130A>C
ENST00000684102.1:n.181A>C
ENST00000684259.1:n.286A>C
ENST00000684479.1:n.102A>C
ENST00000684549.1:n.164A>C
ENST00000684600.1:c.249A>C
ENST00000684670.1:n.102A>C
ENST00000684746.1:n.132A>C
ENST00000261534.9:c.435A>C MANE Select	ENSP00000261534.4:p.Arg145Ser
ENST00000261534.8:c.435A>C	ENSP00000261534.4:p.Arg145Ser
ENST00000452340.7:n.458A>C
ENST00000553863.5:n.102+62A>C
ENST00000554948.1:c.162A>C	ENSP00000452060.1:p.Arg54Ser
ENST00000555675.5:n.151A>C
ENST00000555788.5:n.269A>C
ENST00000556326.5:c.*101A>C	ENSP00000450630.1:n.*101A>C
ENST00000556880.5:n.368A>C
ENST00000557525.1:n.525A>C
NM_013382.5:c.435A>C , LRG_844t1:c.435A>C	NP_037514.2:p.Arg145Ser
XM_011536675.1:c.435A>C	XP_011534977.1:p.Arg145Ser
XM_011536676.1:c.102A>C	XP_011534978.1:p.Arg34Ser
XM_011536677.1:c.435A>C	XP_011534979.1:p.Arg145Ser
XM_011536678.1:c.435A>C	XP_011534980.1:p.Arg145Ser
XM_011536680.1:c.435A>C	XP_011534982.1:p.Arg145Ser
XR_943416.1:n.638A>C
XM_011536675.2:c.435A>C	XP_011534977.1:p.Arg145Ser
XM_011536676.2:c.102A>C	XP_011534978.1:p.Arg34Ser
XM_011536677.3:c.435A>C	XP_011534979.1:p.Arg145Ser
XR_001750279.1:n.635A>C
XR_001750282.1:n.639A>C
XR_943416.3:n.636A>C
NM_013382.6:c.435A>C	NP_037514.2:p.Arg145Ser
NM_013382.7:c.435A>C MANE Select	NP_037514.2:p.Arg145Ser