Canonical Allele Identifier: CA263841607

Gene: POMT2

Linked Data

• dbSNP Id: rs549341255
• gnomAD v3: 14-77306260-G-C
• gnomAD v4: 14-77306260-G-C
• MyVariant Identifiers: chr14:g.77772603G>C (hg19) ; chr14:g.77306260G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306260G>C , CM000676.2:g.77306260G>C	GRCh38
NC_000014.8:g.77772603G>C , CM000676.1:g.77772603G>C	GRCh37
NC_000014.7:g.76842356G>C	NCBI36
NG_008897.1:g.19623C>G , LRG_844:g.19623C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000555675.6:n.244C>G
ENST00000556394.2:c.249-1460C>G	ENSP00000451967.2:n.249-1460C>G
ENST00000556880.6:n.448C>G
ENST00000682247.1:c.438+77C>G	ENSP00000507213.1:n.438+77C>G
ENST00000682382.1:c.386+77C>G
ENST00000682395.1:n.167+77C>G
ENST00000682459.1:n.102+142C>G
ENST00000682467.1:c.438+77C>G	ENSP00000508062.1:n.438+77C>G
ENST00000682795.1:c.438+77C>G	ENSP00000507574.1:n.438+77C>G
ENST00000682895.1:n.154+77C>G
ENST00000682955.1:n.102+142C>G
ENST00000683188.1:c.233+77C>G
ENST00000683380.1:n.102+142C>G
ENST00000683828.1:c.307+77C>G
ENST00000684102.1:n.261C>G
ENST00000684259.1:n.289+77C>G
ENST00000684479.1:n.105+77C>G
ENST00000684549.1:n.244C>G
ENST00000684600.1:c.252+77C>G
ENST00000684670.1:n.105+77C>G
ENST00000261534.9:c.438+77C>G MANE Select	ENSP00000261534.4:n.438+77C>G
ENST00000261534.8:c.438+77C>G	ENSP00000261534.4:n.438+77C>G
ENST00000452340.7:n.461+77C>G
ENST00000553863.5:n.102+142C>G
ENST00000554948.1:c.165+77C>G	ENSP00000452060.1:n.165+77C>G
ENST00000555675.5:n.154+77C>G
ENST00000555788.5:n.349C>G
ENST00000556326.5:c.*104+77C>G	ENSP00000450630.1:n.*104+77C>G
ENST00000556880.5:n.448C>G
ENST00000557525.1:n.528+77C>G
NM_013382.5:c.438+77C>G , LRG_844t1:c.438+77C>G	NP_037514.2:n.438+77C>G
XM_011536675.1:c.438+77C>G	XP_011534977.1:n.438+77C>G
XM_011536676.1:c.105+77C>G	XP_011534978.1:n.105+77C>G
XM_011536677.1:c.438+77C>G	XP_011534979.1:n.438+77C>G
XM_011536678.1:c.438+77C>G	XP_011534980.1:n.438+77C>G
XM_011536679.1:c.-214C>G	XP_011534981.1:n.-214C>G
XM_011536680.1:c.438+77C>G	XP_011534982.1:n.438+77C>G
XR_943416.1:n.641+77C>G
XM_011536675.2:c.438+77C>G	XP_011534977.1:n.438+77C>G
XM_011536676.2:c.105+77C>G	XP_011534978.1:n.105+77C>G
XM_011536677.3:c.438+77C>G	XP_011534979.1:n.438+77C>G
XR_001750279.1:n.638+77C>G
XR_001750282.1:n.642+77C>G
XR_943416.3:n.639+77C>G
NM_013382.6:c.438+77C>G	NP_037514.2:n.438+77C>G
NM_013382.7:c.438+77C>G MANE Select	NP_037514.2:n.438+77C>G