Canonical Allele Identifier: CA2625847637

Gene: POMT2

Linked Data

• gnomAD v4: 14-77306275-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306275A>C , CM000676.2:g.77306275A>C	GRCh38
NC_000014.8:g.77772618A>C , CM000676.1:g.77772618A>C	GRCh37
NC_000014.7:g.76842371A>C	NCBI36
NG_008897.1:g.19608T>G , LRG_844:g.19608T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000555675.6:n.229T>G
ENST00000556394.2:c.249-1475T>G	ENSP00000451967.2:n.249-1475T>G
ENST00000556880.6:n.433T>G
ENST00000682247.1:c.438+62T>G	ENSP00000507213.1:n.438+62T>G
ENST00000682382.1:c.386+62T>G
ENST00000682395.1:n.167+62T>G
ENST00000682459.1:n.102+127T>G
ENST00000682467.1:c.438+62T>G	ENSP00000508062.1:n.438+62T>G
ENST00000682795.1:c.438+62T>G	ENSP00000507574.1:n.438+62T>G
ENST00000682895.1:n.154+62T>G
ENST00000682955.1:n.102+127T>G
ENST00000683188.1:c.233+62T>G
ENST00000683380.1:n.102+127T>G
ENST00000683828.1:c.307+62T>G
ENST00000684102.1:n.246T>G
ENST00000684259.1:n.289+62T>G
ENST00000684479.1:n.105+62T>G
ENST00000684549.1:n.229T>G
ENST00000684600.1:c.252+62T>G
ENST00000684670.1:n.105+62T>G
ENST00000261534.9:c.438+62T>G MANE Select	ENSP00000261534.4:n.438+62T>G
ENST00000261534.8:c.438+62T>G	ENSP00000261534.4:n.438+62T>G
ENST00000452340.7:n.461+62T>G
ENST00000553863.5:n.102+127T>G
ENST00000554948.1:c.165+62T>G	ENSP00000452060.1:n.165+62T>G
ENST00000555675.5:n.154+62T>G
ENST00000555788.5:n.334T>G
ENST00000556326.5:c.*104+62T>G	ENSP00000450630.1:n.*104+62T>G
ENST00000556880.5:n.433T>G
ENST00000557525.1:n.528+62T>G
NM_013382.5:c.438+62T>G , LRG_844t1:c.438+62T>G	NP_037514.2:n.438+62T>G
XM_011536675.1:c.438+62T>G	XP_011534977.1:n.438+62T>G
XM_011536676.1:c.105+62T>G	XP_011534978.1:n.105+62T>G
XM_011536677.1:c.438+62T>G	XP_011534979.1:n.438+62T>G
XM_011536678.1:c.438+62T>G	XP_011534980.1:n.438+62T>G
XM_011536679.1:c.-229T>G	XP_011534981.1:n.-229T>G
XM_011536680.1:c.438+62T>G	XP_011534982.1:n.438+62T>G
XR_943416.1:n.641+62T>G
XM_011536675.2:c.438+62T>G	XP_011534977.1:n.438+62T>G
XM_011536676.2:c.105+62T>G	XP_011534978.1:n.105+62T>G
XM_011536677.3:c.438+62T>G	XP_011534979.1:n.438+62T>G
XR_001750279.1:n.638+62T>G
XR_001750282.1:n.642+62T>G
XR_943416.3:n.639+62T>G
NM_013382.6:c.438+62T>G	NP_037514.2:n.438+62T>G
NM_013382.7:c.438+62T>G MANE Select	NP_037514.2:n.438+62T>G