Canonical Allele Identifier: CA390520376

Gene: POMT2

Linked Data

• gnomAD v4: 14-77301232-C-T
• MyVariant Identifiers: chr14:g.77767575C>T (hg19) ; chr14:g.77301232C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77301232C>T , CM000676.2:g.77301232C>T	GRCh38
NC_000014.8:g.77767575C>T , CM000676.1:g.77767575C>T	GRCh37
NC_000014.7:g.76837328C>T	NCBI36
NG_008897.1:g.24651G>A , LRG_844:g.24651G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553863.6:c.127G>A	ENSP00000508202.1:p.Gly43Ser
ENST00000556394.2:c.358-1671G>A	ENSP00000451967.2:n.358-1671G>A
ENST00000556880.6:n.698G>A
ENST00000557289.2:c.18G>A
ENST00000682247.1:c.674G>A	ENSP00000507213.1:p.Trp225Ter
ENST00000682382.1:c.496-2461G>A
ENST00000682395.1:n.403G>A
ENST00000682459.1:n.338G>A
ENST00000682467.1:c.674G>A	ENSP00000508062.1:p.Trp225Ter
ENST00000682795.1:c.674G>A	ENSP00000507574.1:p.Trp225Ter
ENST00000682895.1:n.390G>A
ENST00000682955.1:n.212-2461G>A
ENST00000683167.1:c.18G>A
ENST00000683188.1:c.343-1671G>A
ENST00000683300.1:c.109+3460G>A	ENSP00000507630.1:n.109+3460G>A
ENST00000683328.1:c.109+3460G>A	ENSP00000508096.1:n.109+3460G>A
ENST00000683380.1:n.338G>A
ENST00000683398.1:c.18G>A
ENST00000683551.1:c.109+1603G>A
ENST00000683828.1:c.525+1603G>A
ENST00000684259.1:n.525G>A
ENST00000684549.1:n.368-1671G>A
ENST00000684554.1:c.18G>A
ENST00000261534.9:c.674G>A MANE Select	ENSP00000261534.4:p.Trp225Ter
ENST00000261534.8:c.674G>A	ENSP00000261534.4:p.Trp225Ter
ENST00000452340.7:n.697G>A
ENST00000553863.5:n.338G>A
ENST00000554948.1:c.401G>A	ENSP00000452060.1:p.Trp134Ter
ENST00000555675.5:n.390G>A
ENST00000556326.5:c.*340G>A	ENSP00000450630.1:n.*340G>A
ENST00000557289.1:c.56-1671G>A	ENSP00000451115.1:n.56-1671G>A
NM_013382.5:c.674G>A , LRG_844t1:c.674G>A	NP_037514.2:p.Trp225Ter
XM_011536675.1:c.674G>A	XP_011534977.1:p.Trp225Ter
XM_011536676.1:c.341G>A	XP_011534978.1:p.Trp114Ter
XM_011536677.1:c.547+3460G>A	XP_011534979.1:n.547+3460G>A
XM_011536678.1:c.674G>A	XP_011534980.1:p.Trp225Ter
XM_011536679.1:c.-90-1671G>A	XP_011534981.1:n.-90-1671G>A
XM_011536680.1:c.674G>A	XP_011534982.1:p.Trp225Ter
XR_943416.1:n.877G>A
XM_011536675.2:c.674G>A	XP_011534977.1:p.Trp225Ter
XM_011536676.2:c.341G>A	XP_011534978.1:p.Trp114Ter
XM_011536677.3:c.547+3460G>A	XP_011534979.1:n.547+3460G>A
XR_001750279.1:n.874G>A
XR_001750282.1:n.878G>A
XR_943416.3:n.875G>A
NM_013382.6:c.674G>A	NP_037514.2:p.Trp225Ter
NM_013382.7:c.674G>A MANE Select	NP_037514.2:p.Trp225Ter