Canonical Allele Identifier: CA2625847501

Gene: POMT2

Linked Data

• gnomAD v4: 14-77306109-TTCTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306115_77306118del , CM000676.2:g.77306115_77306118del	GRCh38
NC_000014.8:g.77772458_77772461del , CM000676.1:g.77772458_77772461del	GRCh37
NC_000014.7:g.76842211_76842214del	NCBI36
NG_008897.1:g.19770_19773del , LRG_844:g.19770_19773del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555675.6:n.391_394del
ENST00000556394.2:c.249-1313_249-1310del	ENSP00000451967.2:n.249-1313_249-1310del
ENST00000556880.6:n.462+133_462+136del
ENST00000682247.1:c.438+224_438+227del	ENSP00000507213.1:n.438+224_438+227del
ENST00000682382.1:c.386+224_386+227del
ENST00000682395.1:n.167+224_167+227del
ENST00000682459.1:n.102+289_102+292del
ENST00000682467.1:c.438+224_438+227del	ENSP00000508062.1:n.438+224_438+227del
ENST00000682795.1:c.438+224_438+227del	ENSP00000507574.1:n.438+224_438+227del
ENST00000682895.1:n.154+224_154+227del
ENST00000682955.1:n.102+289_102+292del
ENST00000683188.1:c.233+224_233+227del
ENST00000683380.1:n.102+289_102+292del
ENST00000683828.1:c.307+224_307+227del
ENST00000684102.1:n.408_411del
ENST00000684259.1:n.289+224_289+227del
ENST00000684479.1:n.105+224_105+227del
ENST00000684549.1:n.258+133_258+136del
ENST00000684600.1:c.252+224_252+227del
ENST00000684670.1:n.105+224_105+227del
ENST00000261534.9:c.438+224_438+227del MANE Select	ENSP00000261534.4:n.438+224_438+227del
ENST00000261534.8:c.438+224_438+227del	ENSP00000261534.4:n.438+224_438+227del
ENST00000452340.7:n.461+224_461+227del
ENST00000553863.5:n.102+289_102+292del
ENST00000554948.1:c.165+224_165+227del	ENSP00000452060.1:n.165+224_165+227del
ENST00000555675.5:n.154+224_154+227del
ENST00000555788.5:n.363+133_363+136del
ENST00000556326.5:c.*104+224_*104+227del	ENSP00000450630.1:n.*104+224_*104+227del
ENST00000556880.5:n.462+133_462+136del
ENST00000557525.1:n.528+224_528+227del
NM_013382.5:c.438+224_438+227del , LRG_844t1:c.438+224_438+227del	NP_037514.2:n.438+224_438+227del
XM_011536675.1:c.438+224_438+227del	XP_011534977.1:n.438+224_438+227del
XM_011536676.1:c.105+224_105+227del	XP_011534978.1:n.105+224_105+227del
XM_011536677.1:c.438+224_438+227del	XP_011534979.1:n.438+224_438+227del
XM_011536678.1:c.438+224_438+227del	XP_011534980.1:n.438+224_438+227del
XM_011536679.1:c.-200+133_-200+136del	XP_011534981.1:n.-200+133_-200+136del
XM_011536680.1:c.438+224_438+227del	XP_011534982.1:n.438+224_438+227del
XR_943416.1:n.641+224_641+227del
XM_011536675.2:c.438+224_438+227del	XP_011534977.1:n.438+224_438+227del
XM_011536676.2:c.105+224_105+227del	XP_011534978.1:n.105+224_105+227del
XM_011536677.3:c.438+224_438+227del	XP_011534979.1:n.438+224_438+227del
XR_001750279.1:n.638+224_638+227del
XR_001750282.1:n.642+224_642+227del
XR_943416.3:n.639+224_639+227del
NM_013382.6:c.438+224_438+227del	NP_037514.2:n.438+224_438+227del
NM_013382.7:c.438+224_438+227del MANE Select	NP_037514.2:n.438+224_438+227del