Canonical Allele Identifier: CA487325248

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77767562G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77301219G>C , CM000676.2:g.77301219G>C	GRCh38
NC_000014.8:g.77767562G>C , CM000676.1:g.77767562G>C	GRCh37
NC_000014.7:g.76837315G>C	NCBI36
NG_008897.1:g.24664C>G , LRG_844:g.24664C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553863.6:c.140C>G	ENSP00000508202.1:p.Ser47Ter
ENST00000556394.2:c.358-1658C>G	ENSP00000451967.2:n.358-1658C>G
ENST00000556880.6:n.711C>G
ENST00000557289.2:c.31C>G
ENST00000682247.1:c.687C>G	ENSP00000507213.1:p.Leu229=
ENST00000682382.1:c.496-2448C>G
ENST00000682395.1:n.416C>G
ENST00000682459.1:n.351C>G
ENST00000682467.1:c.687C>G	ENSP00000508062.1:p.Leu229=
ENST00000682795.1:c.687C>G	ENSP00000507574.1:p.Leu229=
ENST00000682895.1:n.403C>G
ENST00000682955.1:n.212-2448C>G
ENST00000683167.1:c.31C>G
ENST00000683188.1:c.343-1658C>G
ENST00000683300.1:c.109+3473C>G	ENSP00000507630.1:n.109+3473C>G
ENST00000683328.1:c.109+3473C>G	ENSP00000508096.1:n.109+3473C>G
ENST00000683380.1:n.351C>G
ENST00000683398.1:c.31C>G
ENST00000683551.1:c.109+1616C>G
ENST00000683828.1:c.525+1616C>G
ENST00000684259.1:n.538C>G
ENST00000684549.1:n.368-1658C>G
ENST00000684554.1:c.31C>G
ENST00000261534.9:c.687C>G MANE Select	ENSP00000261534.4:p.Leu229=
ENST00000261534.8:c.687C>G	ENSP00000261534.4:p.Leu229=
ENST00000452340.7:n.710C>G
ENST00000553863.5:n.351C>G
ENST00000555675.5:n.403C>G
ENST00000556326.5:c.*353C>G	ENSP00000450630.1:n.*353C>G
ENST00000557289.1:c.56-1658C>G	ENSP00000451115.1:n.56-1658C>G
NM_013382.5:c.687C>G , LRG_844t1:c.687C>G	NP_037514.2:p.Leu229=
XM_011536675.1:c.687C>G	XP_011534977.1:p.Leu229=
XM_011536676.1:c.354C>G	XP_011534978.1:p.Leu118=
XM_011536677.1:c.547+3473C>G	XP_011534979.1:n.547+3473C>G
XM_011536678.1:c.687C>G	XP_011534980.1:p.Leu229=
XM_011536679.1:c.-90-1658C>G	XP_011534981.1:n.-90-1658C>G
XM_011536680.1:c.687C>G	XP_011534982.1:p.Leu229=
XR_943416.1:n.890C>G
XM_011536675.2:c.687C>G	XP_011534977.1:p.Leu229=
XM_011536676.2:c.354C>G	XP_011534978.1:p.Leu118=
XM_011536677.3:c.547+3473C>G	XP_011534979.1:n.547+3473C>G
XR_001750279.1:n.887C>G
XR_001750282.1:n.891C>G
XR_943416.3:n.888C>G
NM_013382.6:c.687C>G	NP_037514.2:p.Leu229=
NM_013382.7:c.687C>G MANE Select	NP_037514.2:p.Leu229=