Canonical Allele Identifier: CA2148328778
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77306218T= , CM000676.2:g.77306218T= GRCh38
NC_000014.8:g.77772561T= , CM000676.1:g.77772561T= GRCh37
NC_000014.7:g.76842314T= NCBI36
NG_008897.1:g.19665A= , LRG_844:g.19665A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555675.6:n.286A=
ENST00000556394.2:c.249-1418A= ENSP00000451967.2:n.249-1418A=
ENST00000556880.6:n.462+28A=
ENST00000682247.1:c.438+119A= ENSP00000507213.1:n.438+119A=
ENST00000682382.1:c.386+119A=
ENST00000682395.1:n.167+119A=
ENST00000682459.1:n.102+184A=
ENST00000682467.1:c.438+119A= ENSP00000508062.1:n.438+119A=
ENST00000682795.1:c.438+119A= ENSP00000507574.1:n.438+119A=
ENST00000682895.1:n.154+119A=
ENST00000682955.1:n.102+184A=
ENST00000683188.1:c.233+119A=
ENST00000683380.1:n.102+184A=
ENST00000683828.1:c.307+119A=
ENST00000684102.1:n.303A=
ENST00000684259.1:n.289+119A=
ENST00000684479.1:n.105+119A=
ENST00000684549.1:n.258+28A=
ENST00000684600.1:c.252+119A=
ENST00000684670.1:n.105+119A=
ENST00000261534.9:c.438+119A= MANE Select ENSP00000261534.4:n.438+119A=
ENST00000261534.8:c.438+119A= ENSP00000261534.4:n.438+119A=
ENST00000452340.7:n.461+119A=
ENST00000553863.5:n.102+184A=
ENST00000554948.1:c.165+119A= ENSP00000452060.1:n.165+119A=
ENST00000555675.5:n.154+119A=
ENST00000555788.5:n.363+28A=
ENST00000556326.5:c.*104+119A= ENSP00000450630.1:n.*104+119A=
ENST00000556880.5:n.462+28A=
ENST00000557525.1:n.528+119A=
NM_013382.5:c.438+119A= , LRG_844t1:c.438+119A= NP_037514.2:n.438+119A=
XM_011536675.1:c.438+119A= XP_011534977.1:n.438+119A=
XM_011536676.1:c.105+119A= XP_011534978.1:n.105+119A=
XM_011536677.1:c.438+119A= XP_011534979.1:n.438+119A=
XM_011536678.1:c.438+119A= XP_011534980.1:n.438+119A=
XM_011536679.1:c.-200+28A= XP_011534981.1:n.-200+28A=
XM_011536680.1:c.438+119A= XP_011534982.1:n.438+119A=
XR_943416.1:n.641+119A=
XM_011536675.2:c.438+119A= XP_011534977.1:n.438+119A=
XM_011536676.2:c.105+119A= XP_011534978.1:n.105+119A=
XM_011536677.3:c.438+119A= XP_011534979.1:n.438+119A=
XR_001750279.1:n.638+119A=
XR_001750282.1:n.642+119A=
XR_943416.3:n.639+119A=
NM_013382.6:c.438+119A= NP_037514.2:n.438+119A=
NM_013382.7:c.438+119A= MANE Select NP_037514.2:n.438+119A=