Canonical Allele Identifier: CA390520366

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77767572C>G (hg19) ; chr14:g.77301229C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77301229C>G , CM000676.2:g.77301229C>G	GRCh38
NC_000014.8:g.77767572C>G , CM000676.1:g.77767572C>G	GRCh37
NC_000014.7:g.76837325C>G	NCBI36
NG_008897.1:g.24654G>C , LRG_844:g.24654G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553863.6:c.130G>C	ENSP00000508202.1:p.Gly44Arg
ENST00000556394.2:c.358-1668G>C	ENSP00000451967.2:n.358-1668G>C
ENST00000556880.6:n.701G>C
ENST00000557289.2:c.21G>C
ENST00000682247.1:c.677G>C	ENSP00000507213.1:p.Trp226Ser
ENST00000682382.1:c.496-2458G>C
ENST00000682395.1:n.406G>C
ENST00000682459.1:n.341G>C
ENST00000682467.1:c.677G>C	ENSP00000508062.1:p.Trp226Ser
ENST00000682795.1:c.677G>C	ENSP00000507574.1:p.Trp226Ser
ENST00000682895.1:n.393G>C
ENST00000682955.1:n.212-2458G>C
ENST00000683167.1:c.21G>C
ENST00000683188.1:c.343-1668G>C
ENST00000683300.1:c.109+3463G>C	ENSP00000507630.1:n.109+3463G>C
ENST00000683328.1:c.109+3463G>C	ENSP00000508096.1:n.109+3463G>C
ENST00000683380.1:n.341G>C
ENST00000683398.1:c.21G>C
ENST00000683551.1:c.109+1606G>C
ENST00000683828.1:c.525+1606G>C
ENST00000684259.1:n.528G>C
ENST00000684549.1:n.368-1668G>C
ENST00000684554.1:c.21G>C
ENST00000261534.9:c.677G>C MANE Select	ENSP00000261534.4:p.Trp226Ser
ENST00000261534.8:c.677G>C	ENSP00000261534.4:p.Trp226Ser
ENST00000452340.7:n.700G>C
ENST00000553863.5:n.341G>C
ENST00000554948.1:c.404G>C	ENSP00000452060.1:p.Trp135Ser
ENST00000555675.5:n.393G>C
ENST00000556326.5:c.*343G>C	ENSP00000450630.1:n.*343G>C
ENST00000557289.1:c.56-1668G>C	ENSP00000451115.1:n.56-1668G>C
NM_013382.5:c.677G>C , LRG_844t1:c.677G>C	NP_037514.2:p.Trp226Ser
XM_011536675.1:c.677G>C	XP_011534977.1:p.Trp226Ser
XM_011536676.1:c.344G>C	XP_011534978.1:p.Trp115Ser
XM_011536677.1:c.547+3463G>C	XP_011534979.1:n.547+3463G>C
XM_011536678.1:c.677G>C	XP_011534980.1:p.Trp226Ser
XM_011536679.1:c.-90-1668G>C	XP_011534981.1:n.-90-1668G>C
XM_011536680.1:c.677G>C	XP_011534982.1:p.Trp226Ser
XR_943416.1:n.880G>C
XM_011536675.2:c.677G>C	XP_011534977.1:p.Trp226Ser
XM_011536676.2:c.344G>C	XP_011534978.1:p.Trp115Ser
XM_011536677.3:c.547+3463G>C	XP_011534979.1:n.547+3463G>C
XR_001750279.1:n.877G>C
XR_001750282.1:n.881G>C
XR_943416.3:n.878G>C
NM_013382.6:c.677G>C	NP_037514.2:p.Trp226Ser
NM_013382.7:c.677G>C MANE Select	NP_037514.2:p.Trp226Ser