Canonical Allele Identifier: CA390520971

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77772706G>T (hg19) ; chr14:g.77306363G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306363G>T , CM000676.2:g.77306363G>T	GRCh38
NC_000014.8:g.77772706G>T , CM000676.1:g.77772706G>T	GRCh37
NC_000014.7:g.76842459G>T	NCBI36
NG_008897.1:g.19520C>A , LRG_844:g.19520C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555675.6:n.141C>A
ENST00000556394.2:c.249-1563C>A	ENSP00000451967.2:n.249-1563C>A
ENST00000556880.6:n.345C>A
ENST00000682247.1:c.412C>A	ENSP00000507213.1:p.His138Asn
ENST00000682382.1:c.360C>A
ENST00000682395.1:n.141C>A
ENST00000682459.1:n.102+39C>A
ENST00000682467.1:c.412C>A	ENSP00000508062.1:p.His138Asn
ENST00000682795.1:c.412C>A	ENSP00000507574.1:p.His138Asn
ENST00000682895.1:n.128C>A
ENST00000682955.1:n.102+39C>A
ENST00000683188.1:c.207C>A
ENST00000683380.1:n.102+39C>A
ENST00000683828.1:c.281C>A
ENST00000684066.1:n.107C>A
ENST00000684102.1:n.158C>A
ENST00000684259.1:n.263C>A
ENST00000684479.1:n.79C>A
ENST00000684549.1:n.141C>A
ENST00000684600.1:c.226C>A
ENST00000684670.1:n.79C>A
ENST00000684746.1:n.109C>A
ENST00000261534.9:c.412C>A MANE Select	ENSP00000261534.4:p.His138Asn
ENST00000261534.8:c.412C>A	ENSP00000261534.4:p.His138Asn
ENST00000452340.7:n.435C>A
ENST00000553863.5:n.102+39C>A
ENST00000554948.1:c.139C>A	ENSP00000452060.1:p.His47Asn
ENST00000555675.5:n.128C>A
ENST00000555788.5:n.246C>A
ENST00000556326.5:c.*78C>A	ENSP00000450630.1:n.*78C>A
ENST00000556880.5:n.345C>A
ENST00000557525.1:n.502C>A
NM_013382.5:c.412C>A , LRG_844t1:c.412C>A	NP_037514.2:p.His138Asn
XM_011536675.1:c.412C>A	XP_011534977.1:p.His138Asn
XM_011536676.1:c.79C>A	XP_011534978.1:p.His27Asn
XM_011536677.1:c.412C>A	XP_011534979.1:p.His138Asn
XM_011536678.1:c.412C>A	XP_011534980.1:p.His138Asn
XM_011536680.1:c.412C>A	XP_011534982.1:p.His138Asn
XR_943416.1:n.615C>A
XM_011536675.2:c.412C>A	XP_011534977.1:p.His138Asn
XM_011536676.2:c.79C>A	XP_011534978.1:p.His27Asn
XM_011536677.3:c.412C>A	XP_011534979.1:p.His138Asn
XR_001750279.1:n.612C>A
XR_001750282.1:n.616C>A
XR_943416.3:n.613C>A
NM_013382.6:c.412C>A	NP_037514.2:p.His138Asn
NM_013382.7:c.412C>A MANE Select	NP_037514.2:p.His138Asn