Canonical Allele Identifier: CA390504318
Community Standard Title: NM_013382.7(POMT2):c.227T>A (p.Leu76Ter)
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77320455A>T , CM000676.2:g.77320455A>T GRCh38
NC_000014.8:g.77786798A>T , CM000676.1:g.77786798A>T GRCh37
NC_000014.7:g.76856551A>T NCBI36
NG_008897.1:g.5428T>A , LRG_844:g.5428T>A

Transcript Alleles

HGVS Amino-acid Change
NM_013382.7:c.227T>A MANE Select NP_037514.2:p.Leu76Ter
ENST00000261534.9:c.227T>A MANE Select ENSP00000261534.4:p.Leu76Ter
NM_013382.5:c.227T>A , LRG_844t1:c.227T>A NP_037514.2:p.Leu76Ter
NM_013382.6:c.227T>A NP_037514.2:p.Leu76Ter
ENST00000261534.8:c.227T>A ENSP00000261534.4:p.Leu76Ter
ENST00000452340.7:n.250T>A
ENST00000556326.5:c.227T>A ENSP00000450630.1:p.Leu76Ter
ENST00000556394.2:c.227T>A ENSP00000451967.2:p.Leu76Ter
ENST00000682247.1:c.227T>A ENSP00000507213.1:p.Leu76Ter
ENST00000682382.1:c.175T>A
ENST00000682467.1:c.227T>A ENSP00000508062.1:p.Leu76Ter
ENST00000682795.1:c.227T>A ENSP00000507574.1:p.Leu76Ter
ENST00000683188.1:c.22T>A
ENST00000683828.1:c.96T>A
ENST00000684344.1:c.227T>A ENSP00000507432.1:p.Leu76Ter
ENST00000684534.1:n.250T>A
XM_011536675.1:c.227T>A XP_011534977.1:p.Leu76Ter
XM_011536675.2:c.227T>A XP_011534977.1:p.Leu76Ter
XM_011536676.1:c.-22T>A XP_011534978.1:n.-22T>A
XM_011536676.2:c.-22T>A XP_011534978.1:n.-22T>A
XM_011536677.1:c.227T>A XP_011534979.1:p.Leu76Ter
XM_011536677.3:c.227T>A XP_011534979.1:p.Leu76Ter
XM_011536678.1:c.227T>A XP_011534980.1:p.Leu76Ter
XM_011536680.1:c.227T>A XP_011534982.1:p.Leu76Ter
XR_001750279.1:n.427T>A
XR_001750282.1:n.431T>A
XR_943416.1:n.430T>A
XR_943416.3:n.428T>A