Canonical Allele Identifier: CA390520951

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77772699C>G (hg19) ; chr14:g.77306356C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306356C>G , CM000676.2:g.77306356C>G	GRCh38
NC_000014.8:g.77772699C>G , CM000676.1:g.77772699C>G	GRCh37
NC_000014.7:g.76842452C>G	NCBI36
NG_008897.1:g.19527G>C , LRG_844:g.19527G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555675.6:n.148G>C
ENST00000556394.2:c.249-1556G>C	ENSP00000451967.2:n.249-1556G>C
ENST00000556880.6:n.352G>C
ENST00000682247.1:c.419G>C	ENSP00000507213.1:p.Ser140Thr
ENST00000682382.1:c.367G>C
ENST00000682395.1:n.148G>C
ENST00000682459.1:n.102+46G>C
ENST00000682467.1:c.419G>C	ENSP00000508062.1:p.Ser140Thr
ENST00000682795.1:c.419G>C	ENSP00000507574.1:p.Ser140Thr
ENST00000682895.1:n.135G>C
ENST00000682955.1:n.102+46G>C
ENST00000683188.1:c.214G>C
ENST00000683380.1:n.102+46G>C
ENST00000683828.1:c.288G>C
ENST00000684066.1:n.114G>C
ENST00000684102.1:n.165G>C
ENST00000684259.1:n.270G>C
ENST00000684479.1:n.86G>C
ENST00000684549.1:n.148G>C
ENST00000684600.1:c.233G>C
ENST00000684670.1:n.86G>C
ENST00000684746.1:n.116G>C
ENST00000261534.9:c.419G>C MANE Select	ENSP00000261534.4:p.Ser140Thr
ENST00000261534.8:c.419G>C	ENSP00000261534.4:p.Ser140Thr
ENST00000452340.7:n.442G>C
ENST00000553863.5:n.102+46G>C
ENST00000554948.1:c.146G>C	ENSP00000452060.1:p.Ser49Thr
ENST00000555675.5:n.135G>C
ENST00000555788.5:n.253G>C
ENST00000556326.5:c.*85G>C	ENSP00000450630.1:n.*85G>C
ENST00000556880.5:n.352G>C
ENST00000557525.1:n.509G>C
NM_013382.5:c.419G>C , LRG_844t1:c.419G>C	NP_037514.2:p.Ser140Thr
XM_011536675.1:c.419G>C	XP_011534977.1:p.Ser140Thr
XM_011536676.1:c.86G>C	XP_011534978.1:p.Ser29Thr
XM_011536677.1:c.419G>C	XP_011534979.1:p.Ser140Thr
XM_011536678.1:c.419G>C	XP_011534980.1:p.Ser140Thr
XM_011536680.1:c.419G>C	XP_011534982.1:p.Ser140Thr
XR_943416.1:n.622G>C
XM_011536675.2:c.419G>C	XP_011534977.1:p.Ser140Thr
XM_011536676.2:c.86G>C	XP_011534978.1:p.Ser29Thr
XM_011536677.3:c.419G>C	XP_011534979.1:p.Ser140Thr
XR_001750279.1:n.619G>C
XR_001750282.1:n.623G>C
XR_943416.3:n.620G>C
NM_013382.6:c.419G>C	NP_037514.2:p.Ser140Thr
NM_013382.7:c.419G>C MANE Select	NP_037514.2:p.Ser140Thr