Canonical Allele Identifier: CA390520946

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77772697A>C (hg19) ; chr14:g.77306354A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306354A>C , CM000676.2:g.77306354A>C	GRCh38
NC_000014.8:g.77772697A>C , CM000676.1:g.77772697A>C	GRCh37
NC_000014.7:g.76842450A>C	NCBI36
NG_008897.1:g.19529T>G , LRG_844:g.19529T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555675.6:n.150T>G
ENST00000556394.2:c.249-1554T>G	ENSP00000451967.2:n.249-1554T>G
ENST00000556880.6:n.354T>G
ENST00000682247.1:c.421T>G	ENSP00000507213.1:p.Tyr141Asp
ENST00000682382.1:c.369T>G
ENST00000682395.1:n.150T>G
ENST00000682459.1:n.102+48T>G
ENST00000682467.1:c.421T>G	ENSP00000508062.1:p.Tyr141Asp
ENST00000682795.1:c.421T>G	ENSP00000507574.1:p.Tyr141Asp
ENST00000682895.1:n.137T>G
ENST00000682955.1:n.102+48T>G
ENST00000683188.1:c.216T>G
ENST00000683380.1:n.102+48T>G
ENST00000683828.1:c.290T>G
ENST00000684066.1:n.116T>G
ENST00000684102.1:n.167T>G
ENST00000684259.1:n.272T>G
ENST00000684479.1:n.88T>G
ENST00000684549.1:n.150T>G
ENST00000684600.1:c.235T>G
ENST00000684670.1:n.88T>G
ENST00000684746.1:n.118T>G
ENST00000261534.9:c.421T>G MANE Select	ENSP00000261534.4:p.Tyr141Asp
ENST00000261534.8:c.421T>G	ENSP00000261534.4:p.Tyr141Asp
ENST00000452340.7:n.444T>G
ENST00000553863.5:n.102+48T>G
ENST00000554948.1:c.148T>G	ENSP00000452060.1:p.Tyr50Asp
ENST00000555675.5:n.137T>G
ENST00000555788.5:n.255T>G
ENST00000556326.5:c.*87T>G	ENSP00000450630.1:n.*87T>G
ENST00000556880.5:n.354T>G
ENST00000557525.1:n.511T>G
NM_013382.5:c.421T>G , LRG_844t1:c.421T>G	NP_037514.2:p.Tyr141Asp
XM_011536675.1:c.421T>G	XP_011534977.1:p.Tyr141Asp
XM_011536676.1:c.88T>G	XP_011534978.1:p.Tyr30Asp
XM_011536677.1:c.421T>G	XP_011534979.1:p.Tyr141Asp
XM_011536678.1:c.421T>G	XP_011534980.1:p.Tyr141Asp
XM_011536680.1:c.421T>G	XP_011534982.1:p.Tyr141Asp
XR_943416.1:n.624T>G
XM_011536675.2:c.421T>G	XP_011534977.1:p.Tyr141Asp
XM_011536676.2:c.88T>G	XP_011534978.1:p.Tyr30Asp
XM_011536677.3:c.421T>G	XP_011534979.1:p.Tyr141Asp
XR_001750279.1:n.621T>G
XR_001750282.1:n.625T>G
XR_943416.3:n.622T>G
NM_013382.6:c.421T>G	NP_037514.2:p.Tyr141Asp
NM_013382.7:c.421T>G MANE Select	NP_037514.2:p.Tyr141Asp