Canonical Allele Identifier: CA390518954
Community Standard Title: NM_013382.7(POMT2):c.1130T>A (p.Leu377Ter)
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77291367A>T , CM000676.2:g.77291367A>T GRCh38
NC_000014.8:g.77757710A>T , CM000676.1:g.77757710A>T GRCh37
NC_000014.7:g.76827463A>T NCBI36
NG_008897.1:g.34516T>A , LRG_844:g.34516T>A

Transcript Alleles

HGVS Amino-acid Change
NM_013382.7:c.1130T>A MANE Select NP_037514.2:p.Leu377Ter
ENST00000261534.9:c.1130T>A MANE Select ENSP00000261534.4:p.Leu377Ter
NM_013382.5:c.1130T>A , LRG_844t1:c.1130T>A NP_037514.2:p.Leu377Ter
NM_013382.6:c.1130T>A NP_037514.2:p.Leu377Ter
ENST00000261534.8:c.1130T>A ENSP00000261534.4:p.Leu377Ter
ENST00000452340.7:n.1153T>A
ENST00000553880.5:n.1T>A
ENST00000554767.5:n.1916T>A
ENST00000556394.2:c.671T>A ENSP00000451967.2:p.Leu224Ter
ENST00000556851.1:n.127T>A
ENST00000557675.5:n.220T>A
ENST00000682247.1:c.1130T>A ENSP00000507213.1:p.Leu377Ter
ENST00000682382.1:c.702T>A
ENST00000682395.1:n.859T>A
ENST00000682459.1:n.794T>A
ENST00000682467.1:c.1130T>A ENSP00000508062.1:p.Leu377Ter
ENST00000682795.1:c.1130T>A ENSP00000507574.1:p.Leu377Ter
ENST00000682895.1:n.846T>A
ENST00000682955.1:n.418T>A
ENST00000683188.1:c.656T>A
ENST00000683285.1:c.275T>A
ENST00000683328.1:c.123T>A ENSP00000508096.1:p.Phe41Leu
ENST00000683380.1:n.794T>A
ENST00000683828.1:c.839T>A
ENST00000684259.1:n.981T>A
ENST00000684528.1:c.645T>A
ENST00000684549.1:n.681T>A
XM_011536675.1:c.1130T>A XP_011534977.1:p.Leu377Ter
XM_011536675.2:c.1130T>A XP_011534977.1:p.Leu377Ter
XM_011536676.1:c.797T>A XP_011534978.1:p.Leu266Ter
XM_011536676.2:c.797T>A XP_011534978.1:p.Leu266Ter
XM_011536677.1:c.671T>A XP_011534979.1:p.Leu224Ter
XM_011536677.3:c.671T>A XP_011534979.1:p.Leu224Ter
XM_011536678.1:c.1130T>A XP_011534980.1:p.Leu377Ter
XM_011536679.1:c.224T>A XP_011534981.1:p.Leu75Ter
XM_011536680.1:c.1130T>A XP_011534982.1:p.Leu377Ter
XR_001750279.1:n.1330T>A
XR_001750282.1:n.1334T>A
XR_943416.1:n.1333T>A
XR_943416.3:n.1331T>A