Canonical Allele Identifier: CA2625846240
Gene: POMT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77279056C>T , CM000676.2:g.77279056C>T GRCh38
NC_000014.8:g.77745399C>T , CM000676.1:g.77745399C>T GRCh37
NC_000014.7:g.76815152C>T NCBI36
NG_008897.1:g.46827G>A , LRG_844:g.46827G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.817-187G>A
ENST00000556394.2:c.1433-187G>A ENSP00000451967.2:n.1433-187G>A
ENST00000682128.1:c.193-187G>A ENSP00000506976.1:n.193-187G>A
ENST00000682247.1:c.1892-198G>A ENSP00000507213.1:n.1892-198G>A
ENST00000682395.1:n.2356-187G>A
ENST00000682459.1:n.1595-187G>A
ENST00000682467.1:c.1892-548G>A ENSP00000508062.1:n.1892-548G>A
ENST00000682615.1:n.246-187G>A
ENST00000682795.1:c.2039-187G>A ENSP00000507574.1:n.2039-187G>A
ENST00000682895.1:n.1608-187G>A
ENST00000682955.1:n.1466-187G>A
ENST00000683095.1:c.298-187G>A ENSP00000508040.1:n.298-187G>A
ENST00000683188.1:c.2153-187G>A
ENST00000683380.1:n.1556-187G>A
ENST00000683828.1:c.1601-187G>A
ENST00000683907.1:c.157-187G>A ENSP00000507754.1:n.157-187G>A
ENST00000684172.1:c.268-187G>A ENSP00000508391.1:n.268-187G>A
ENST00000684259.1:n.3472G>A
ENST00000684538.1:n.1084G>A
ENST00000684549.1:n.1443-187G>A
ENST00000261534.9:c.1892-187G>A MANE Select ENSP00000261534.4:n.1892-187G>A
ENST00000261534.8:c.1892-187G>A ENSP00000261534.4:n.1892-187G>A
ENST00000452340.7:n.2681G>A
ENST00000554767.5:n.2678-187G>A
ENST00000555134.1:n.817-187G>A
ENST00000555710.1:c.161-95G>A ENSP00000451730.1:n.161-95G>A
ENST00000556171.1:c.484-187G>A
ENST00000556394.1:c.88-548G>A
ENST00000556446.1:n.6G>A
ENST00000602717.5:c.107-187G>A ENSP00000487704.1:n.107-187G>A
NM_013382.5:c.1892-187G>A , LRG_844t1:c.1892-187G>A NP_037514.2:n.1892-187G>A
XM_011536675.1:c.2081-187G>A XP_011534977.1:n.2081-187G>A
XM_011536676.1:c.1748-187G>A XP_011534978.1:n.1748-187G>A
XM_011536677.1:c.1622-187G>A XP_011534979.1:n.1622-187G>A
XM_011536678.1:c.*442G>A XP_011534980.1:n.*442G>A
XM_011536679.1:c.1175-187G>A XP_011534981.1:n.1175-187G>A
XR_943416.1:n.2145-187G>A
XM_011536675.2:c.2081-187G>A XP_011534977.1:n.2081-187G>A
XM_011536676.2:c.1748-187G>A XP_011534978.1:n.1748-187G>A
XM_011536677.3:c.1622-187G>A XP_011534979.1:n.1622-187G>A
XR_001750279.1:n.2178-187G>A
XR_001750282.1:n.2831-187G>A
XR_943416.3:n.2143-187G>A
NM_013382.6:c.1892-187G>A NP_037514.2:n.1892-187G>A
NM_013382.7:c.1892-187G>A MANE Select NP_037514.2:n.1892-187G>A