Canonical Allele Identifier: CA390520369

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77767573A>G (hg19) ; chr14:g.77301230A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77301230A>G , CM000676.2:g.77301230A>G	GRCh38
NC_000014.8:g.77767573A>G , CM000676.1:g.77767573A>G	GRCh37
NC_000014.7:g.76837326A>G	NCBI36
NG_008897.1:g.24653T>C , LRG_844:g.24653T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553863.6:c.129T>C	ENSP00000508202.1:p.Gly43=
ENST00000556394.2:c.358-1669T>C	ENSP00000451967.2:n.358-1669T>C
ENST00000556880.6:n.700T>C
ENST00000557289.2:c.20T>C
ENST00000682247.1:c.676T>C	ENSP00000507213.1:p.Trp226Arg
ENST00000682382.1:c.496-2459T>C
ENST00000682395.1:n.405T>C
ENST00000682459.1:n.340T>C
ENST00000682467.1:c.676T>C	ENSP00000508062.1:p.Trp226Arg
ENST00000682795.1:c.676T>C	ENSP00000507574.1:p.Trp226Arg
ENST00000682895.1:n.392T>C
ENST00000682955.1:n.212-2459T>C
ENST00000683167.1:c.20T>C
ENST00000683188.1:c.343-1669T>C
ENST00000683300.1:c.109+3462T>C	ENSP00000507630.1:n.109+3462T>C
ENST00000683328.1:c.109+3462T>C	ENSP00000508096.1:n.109+3462T>C
ENST00000683380.1:n.340T>C
ENST00000683398.1:c.20T>C
ENST00000683551.1:c.109+1605T>C
ENST00000683828.1:c.525+1605T>C
ENST00000684259.1:n.527T>C
ENST00000684549.1:n.368-1669T>C
ENST00000684554.1:c.20T>C
ENST00000261534.9:c.676T>C MANE Select	ENSP00000261534.4:p.Trp226Arg
ENST00000261534.8:c.676T>C	ENSP00000261534.4:p.Trp226Arg
ENST00000452340.7:n.699T>C
ENST00000553863.5:n.340T>C
ENST00000554948.1:c.403T>C	ENSP00000452060.1:p.Trp135Arg
ENST00000555675.5:n.392T>C
ENST00000556326.5:c.*342T>C	ENSP00000450630.1:n.*342T>C
ENST00000557289.1:c.56-1669T>C	ENSP00000451115.1:n.56-1669T>C
NM_013382.5:c.676T>C , LRG_844t1:c.676T>C	NP_037514.2:p.Trp226Arg
XM_011536675.1:c.676T>C	XP_011534977.1:p.Trp226Arg
XM_011536676.1:c.343T>C	XP_011534978.1:p.Trp115Arg
XM_011536677.1:c.547+3462T>C	XP_011534979.1:n.547+3462T>C
XM_011536678.1:c.676T>C	XP_011534980.1:p.Trp226Arg
XM_011536679.1:c.-90-1669T>C	XP_011534981.1:n.-90-1669T>C
XM_011536680.1:c.676T>C	XP_011534982.1:p.Trp226Arg
XR_943416.1:n.879T>C
XM_011536675.2:c.676T>C	XP_011534977.1:p.Trp226Arg
XM_011536676.2:c.343T>C	XP_011534978.1:p.Trp115Arg
XM_011536677.3:c.547+3462T>C	XP_011534979.1:n.547+3462T>C
XR_001750279.1:n.876T>C
XR_001750282.1:n.880T>C
XR_943416.3:n.877T>C
NM_013382.6:c.676T>C	NP_037514.2:p.Trp226Arg
NM_013382.7:c.676T>C MANE Select	NP_037514.2:p.Trp226Arg