Canonical Allele Identifier: CA390519665
Gene: POMT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77298691T>G , CM000676.2:g.77298691T>G GRCh38
NC_000014.8:g.77765034T>G , CM000676.1:g.77765034T>G GRCh37
NC_000014.7:g.76834787T>G NCBI36
NG_008897.1:g.27192A>C , LRG_844:g.27192A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000556394.2:c.545A>C ENSP00000451967.2:p.Glu182Ala
ENST00000557289.2:c.302A>C
ENST00000682247.1:c.1004A>C ENSP00000507213.1:p.Glu335Ala
ENST00000682382.1:c.576A>C
ENST00000682395.1:n.733A>C
ENST00000682459.1:n.668A>C
ENST00000682467.1:c.1004A>C ENSP00000508062.1:p.Glu335Ala
ENST00000682795.1:c.1004A>C ENSP00000507574.1:p.Glu335Ala
ENST00000682895.1:n.720A>C
ENST00000682955.1:n.292A>C
ENST00000683188.1:c.530A>C
ENST00000683300.1:c.110-2418A>C ENSP00000507630.1:n.110-2418A>C
ENST00000683328.1:c.109+6001A>C ENSP00000508096.1:n.109+6001A>C
ENST00000683380.1:n.668A>C
ENST00000683551.1:c.190A>C
ENST00000683828.1:c.713A>C
ENST00000684259.1:n.855A>C
ENST00000684549.1:n.555A>C
ENST00000684554.1:c.241A>C
ENST00000261534.9:c.1004A>C MANE Select ENSP00000261534.4:p.Glu335Ala
ENST00000261534.8:c.1004A>C ENSP00000261534.4:p.Glu335Ala
ENST00000452340.7:n.1027A>C
ENST00000554767.5:n.1790A>C
ENST00000557289.1:c.243A>C ENSP00000451115.1:n.243A>C
NM_013382.5:c.1004A>C , LRG_844t1:c.1004A>C NP_037514.2:p.Glu335Ala
XM_011536675.1:c.1004A>C XP_011534977.1:p.Glu335Ala
XM_011536676.1:c.671A>C XP_011534978.1:p.Glu224Ala
XM_011536677.1:c.548-2418A>C XP_011534979.1:n.548-2418A>C
XM_011536678.1:c.1004A>C XP_011534980.1:p.Glu335Ala
XM_011536679.1:c.98A>C XP_011534981.1:p.Glu33Ala
XM_011536680.1:c.1004A>C XP_011534982.1:p.Glu335Ala
XR_943416.1:n.1207A>C
XM_011536675.2:c.1004A>C XP_011534977.1:p.Glu335Ala
XM_011536676.2:c.671A>C XP_011534978.1:p.Glu224Ala
XM_011536677.3:c.548-2418A>C XP_011534979.1:n.548-2418A>C
XR_001750279.1:n.1204A>C
XR_001750282.1:n.1208A>C
XR_943416.3:n.1205A>C
NM_013382.6:c.1004A>C NP_037514.2:p.Glu335Ala
NM_013382.7:c.1004A>C MANE Select NP_037514.2:p.Glu335Ala