Canonical Allele Identifier: CA2625845467
Gene: POMT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278634C>T , CM000676.2:g.77278634C>T GRCh38
NC_000014.8:g.77744977C>T , CM000676.1:g.77744977C>T GRCh37
NC_000014.7:g.76814730C>T NCBI36
NG_008897.1:g.47249G>A , LRG_844:g.47249G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.957+95G>A
ENST00000556394.2:c.1573+95G>A ENSP00000451967.2:n.1573+95G>A
ENST00000682247.1:c.2021+95G>A ENSP00000507213.1:n.2021+95G>A
ENST00000682395.1:n.2496+95G>A
ENST00000682459.1:n.1735+95G>A
ENST00000682467.1:c.1892-126G>A ENSP00000508062.1:n.1892-126G>A
ENST00000682795.1:c.2179+95G>A ENSP00000507574.1:n.2179+95G>A
ENST00000682895.1:n.1748+95G>A
ENST00000682955.1:n.1606+95G>A
ENST00000683188.1:c.2293+95G>A
ENST00000683380.1:n.1696+95G>A
ENST00000683907.1:c.297+95G>A ENSP00000507754.1:n.297+95G>A
ENST00000684259.1:n.3799+95G>A
ENST00000684538.1:n.1411+95G>A
ENST00000684549.1:n.1583+95G>A
ENST00000261534.9:c.2032+95G>A MANE Select ENSP00000261534.4:n.2032+95G>A
ENST00000261534.8:c.2032+95G>A ENSP00000261534.4:n.2032+95G>A
ENST00000452340.7:n.3008+95G>A
ENST00000554767.5:n.2818+95G>A
ENST00000555710.1:c.393+95G>A ENSP00000451730.1:n.393+95G>A
ENST00000556394.1:c.88-126G>A
ENST00000556446.1:n.333+95G>A
ENST00000602717.5:c.247+95G>A ENSP00000487704.1:n.247+95G>A
NM_013382.5:c.2032+95G>A , LRG_844t1:c.2032+95G>A NP_037514.2:n.2032+95G>A
XM_011536675.1:c.2221+95G>A XP_011534977.1:n.2221+95G>A
XM_011536676.1:c.1888+95G>A XP_011534978.1:n.1888+95G>A
XM_011536677.1:c.1762+95G>A XP_011534979.1:n.1762+95G>A
XM_011536679.1:c.1315+95G>A XP_011534981.1:n.1315+95G>A
XR_943416.1:n.2285+95G>A
XM_011536675.2:c.2221+95G>A XP_011534977.1:n.2221+95G>A
XM_011536676.2:c.1888+95G>A XP_011534978.1:n.1888+95G>A
XM_011536677.3:c.1762+95G>A XP_011534979.1:n.1762+95G>A
XR_001750279.1:n.2318+95G>A
XR_001750282.1:n.2971+95G>A
XR_943416.3:n.2283+95G>A
NM_013382.6:c.2032+95G>A NP_037514.2:n.2032+95G>A
NM_013382.7:c.2032+95G>A MANE Select NP_037514.2:n.2032+95G>A