Canonical Allele Identifier: CA2625846330
Gene: POMT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77279144C>A , CM000676.2:g.77279144C>A GRCh38
NC_000014.8:g.77745487C>A , CM000676.1:g.77745487C>A GRCh37
NC_000014.7:g.76815240C>A NCBI36
NG_008897.1:g.46739G>T , LRG_844:g.46739G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.817-275G>T
ENST00000556394.2:c.1433-275G>T ENSP00000451967.2:n.1433-275G>T
ENST00000682128.1:c.193-275G>T ENSP00000506976.1:n.193-275G>T
ENST00000682247.1:c.1892-286G>T ENSP00000507213.1:n.1892-286G>T
ENST00000682395.1:n.2356-275G>T
ENST00000682459.1:n.1595-275G>T
ENST00000682467.1:c.1892-636G>T ENSP00000508062.1:n.1892-636G>T
ENST00000682615.1:n.246-275G>T
ENST00000682795.1:c.2039-275G>T ENSP00000507574.1:n.2039-275G>T
ENST00000682895.1:n.1608-275G>T
ENST00000682955.1:n.1466-275G>T
ENST00000683095.1:c.298-275G>T ENSP00000508040.1:n.298-275G>T
ENST00000683188.1:c.2153-275G>T
ENST00000683380.1:n.1556-275G>T
ENST00000683828.1:c.1601-275G>T
ENST00000683907.1:c.157-275G>T ENSP00000507754.1:n.157-275G>T
ENST00000684172.1:c.268-275G>T ENSP00000508391.1:n.268-275G>T
ENST00000684259.1:n.3384G>T
ENST00000684538.1:n.996G>T
ENST00000684549.1:n.1443-275G>T
ENST00000261534.9:c.1892-275G>T MANE Select ENSP00000261534.4:n.1892-275G>T
ENST00000261534.8:c.1892-275G>T ENSP00000261534.4:n.1892-275G>T
ENST00000452340.7:n.2593G>T
ENST00000554767.5:n.2678-275G>T
ENST00000555134.1:n.817-275G>T
ENST00000555710.1:c.161-183G>T ENSP00000451730.1:n.161-183G>T
ENST00000556171.1:c.484-275G>T
ENST00000556394.1:c.88-636G>T
ENST00000602717.5:c.107-275G>T ENSP00000487704.1:n.107-275G>T
NM_013382.5:c.1892-275G>T , LRG_844t1:c.1892-275G>T NP_037514.2:n.1892-275G>T
XM_011536675.1:c.2081-275G>T XP_011534977.1:n.2081-275G>T
XM_011536676.1:c.1748-275G>T XP_011534978.1:n.1748-275G>T
XM_011536677.1:c.1622-275G>T XP_011534979.1:n.1622-275G>T
XM_011536678.1:c.*354G>T XP_011534980.1:n.*354G>T
XM_011536679.1:c.1175-275G>T XP_011534981.1:n.1175-275G>T
XR_943416.1:n.2145-275G>T
XM_011536675.2:c.2081-275G>T XP_011534977.1:n.2081-275G>T
XM_011536676.2:c.1748-275G>T XP_011534978.1:n.1748-275G>T
XM_011536677.3:c.1622-275G>T XP_011534979.1:n.1622-275G>T
XR_001750279.1:n.2178-275G>T
XR_001750282.1:n.2831-275G>T
XR_943416.3:n.2143-275G>T
NM_013382.6:c.1892-275G>T NP_037514.2:n.1892-275G>T
NM_013382.7:c.1892-275G>T MANE Select NP_037514.2:n.1892-275G>T