Canonical Allele Identifier: CA2625844181
Gene: POMT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77286995G>A , CM000676.2:g.77286995G>A GRCh38
NC_000014.8:g.77753338G>A , CM000676.1:g.77753338G>A GRCh37
NC_000014.7:g.76823091G>A NCBI36
NG_008897.1:g.38888C>T , LRG_844:g.38888C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000556394.2:c.795-173C>T ENSP00000451967.2:n.795-173C>T
ENST00000682247.1:c.1254-173C>T ENSP00000507213.1:n.1254-173C>T
ENST00000682382.1:c.826-173C>T
ENST00000682395.1:n.1259C>T
ENST00000682459.1:n.957-173C>T
ENST00000682467.1:c.1254-173C>T ENSP00000508062.1:n.1254-173C>T
ENST00000682706.1:n.18C>T
ENST00000682795.1:c.1254-173C>T ENSP00000507574.1:n.1254-173C>T
ENST00000682895.1:n.970-173C>T
ENST00000682955.1:n.542-173C>T
ENST00000683188.1:c.1056C>T
ENST00000683328.1:c.247-173C>T ENSP00000508096.1:n.247-173C>T
ENST00000683380.1:n.918-173C>T
ENST00000683828.1:c.963-173C>T
ENST00000684259.1:n.1105-173C>T
ENST00000684549.1:n.805-173C>T
ENST00000261534.9:c.1254-173C>T MANE Select ENSP00000261534.4:n.1254-173C>T
ENST00000261534.8:c.1254-173C>T ENSP00000261534.4:n.1254-173C>T
ENST00000452340.7:n.1277-173C>T
ENST00000553880.5:n.125-173C>T
ENST00000554767.5:n.2040-173C>T
ENST00000554884.5:n.246-173C>T
ENST00000556404.1:n.215C>T
ENST00000556851.1:n.290-173C>T
ENST00000557675.5:n.344-173C>T
NM_013382.5:c.1254-173C>T , LRG_844t1:c.1254-173C>T NP_037514.2:n.1254-173C>T
XM_011536675.1:c.1254-173C>T XP_011534977.1:n.1254-173C>T
XM_011536676.1:c.921-173C>T XP_011534978.1:n.921-173C>T
XM_011536677.1:c.795-173C>T XP_011534979.1:n.795-173C>T
XM_011536678.1:c.1254-173C>T XP_011534980.1:n.1254-173C>T
XM_011536679.1:c.348-173C>T XP_011534981.1:n.348-173C>T
XM_011536680.1:c.*234C>T XP_011534982.1:n.*234C>T
XR_943416.1:n.1457-173C>T
XM_011536675.2:c.1254-173C>T XP_011534977.1:n.1254-173C>T
XM_011536676.2:c.921-173C>T XP_011534978.1:n.921-173C>T
XM_011536677.3:c.795-173C>T XP_011534979.1:n.795-173C>T
XR_001750279.1:n.1454-173C>T
XR_001750282.1:n.1734C>T
XR_943416.3:n.1455-173C>T
NM_013382.6:c.1254-173C>T NP_037514.2:n.1254-173C>T
NM_013382.7:c.1254-173C>T MANE Select NP_037514.2:n.1254-173C>T