Canonical Allele Identifier: CA2148327483
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278466A= , CM000676.2:g.77278466A= GRCh38
NC_000014.8:g.77744809A= , CM000676.1:g.77744809A= GRCh37
NC_000014.7:g.76814562A= NCBI36
NG_008897.1:g.47417T= , LRG_844:g.47417T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.1000T=
ENST00000556394.2:c.1616T= ENSP00000451967.2:p.Leu539=
ENST00000682247.1:c.2064T= ENSP00000507213.1:p.Leu688=
ENST00000682395.1:n.2539T=
ENST00000682459.1:n.1778T=
ENST00000682467.1:c.1934T= ENSP00000508062.1:p.Leu645=
ENST00000682795.1:c.2222T= ENSP00000507574.1:p.Leu741=
ENST00000682895.1:n.1791T=
ENST00000682955.1:n.1649T=
ENST00000683188.1:c.2336T=
ENST00000683380.1:n.1739T=
ENST00000683907.1:c.340T= ENSP00000507754.1:n.340T=
ENST00000684259.1:n.3842T=
ENST00000684538.1:n.1454T=
ENST00000684549.1:n.1626T=
ENST00000261534.9:c.2075T= MANE Select ENSP00000261534.4:p.Leu692=
ENST00000261534.8:c.2075T= ENSP00000261534.4:p.Leu692=
ENST00000452340.7:n.3051T=
ENST00000554767.5:n.2861T=
ENST00000555710.1:c.436T= ENSP00000451730.1:n.436T=
ENST00000556394.1:c.130T=
ENST00000556446.1:n.376T=
ENST00000602717.5:c.290T= ENSP00000487704.1:p.Leu97=
NM_013382.5:c.2075T= , LRG_844t1:c.2075T= NP_037514.2:p.Leu692=
XM_011536675.1:c.2264T= XP_011534977.1:p.Leu755=
XM_011536676.1:c.1931T= XP_011534978.1:p.Leu644=
XM_011536677.1:c.1805T= XP_011534979.1:p.Leu602=
XM_011536679.1:c.1358T= XP_011534981.1:p.Leu453=
XR_943416.1:n.2328T=
XM_011536675.2:c.2264T= XP_011534977.1:p.Leu755=
XM_011536676.2:c.1931T= XP_011534978.1:p.Leu644=
XM_011536677.3:c.1805T= XP_011534979.1:p.Leu602=
XR_001750279.1:n.2361T=
XR_001750282.1:n.3014T=
XR_943416.3:n.2326T=
NM_013382.6:c.2075T= NP_037514.2:p.Leu692=
NM_013382.7:c.2075T= MANE Select NP_037514.2:p.Leu692=