Canonical Allele Identifier: CA487325114

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77767448G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77301105G>A , CM000676.2:g.77301105G>A	GRCh38
NC_000014.8:g.77767448G>A , CM000676.1:g.77767448G>A	GRCh37
NC_000014.7:g.76837201G>A	NCBI36
NG_008897.1:g.24778C>T , LRG_844:g.24778C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553863.6:c.254C>T	ENSP00000508202.1:n.254C>T
ENST00000556394.2:c.358-1544C>T	ENSP00000451967.2:n.358-1544C>T
ENST00000557289.2:c.145C>T
ENST00000682247.1:c.801C>T	ENSP00000507213.1:p.Asp267=
ENST00000682382.1:c.496-2334C>T
ENST00000682395.1:n.530C>T
ENST00000682459.1:n.465C>T
ENST00000682467.1:c.801C>T	ENSP00000508062.1:p.Asp267=
ENST00000682795.1:c.801C>T	ENSP00000507574.1:p.Asp267=
ENST00000682895.1:n.517C>T
ENST00000682955.1:n.212-2334C>T
ENST00000683167.1:c.145C>T
ENST00000683188.1:c.343-1544C>T
ENST00000683300.1:c.109+3587C>T	ENSP00000507630.1:n.109+3587C>T
ENST00000683328.1:c.109+3587C>T	ENSP00000508096.1:n.109+3587C>T
ENST00000683380.1:n.465C>T
ENST00000683398.1:c.145C>T
ENST00000683551.1:c.109+1730C>T
ENST00000683828.1:c.526-1544C>T
ENST00000684259.1:n.652C>T
ENST00000684549.1:n.368-1544C>T
ENST00000684554.1:c.145C>T
ENST00000261534.9:c.801C>T MANE Select	ENSP00000261534.4:p.Asp267=
ENST00000261534.8:c.801C>T	ENSP00000261534.4:p.Asp267=
ENST00000452340.7:n.824C>T
ENST00000553863.5:n.465C>T
ENST00000554767.5:n.59C>T
ENST00000555675.5:n.517C>T
ENST00000556326.5:c.*467C>T	ENSP00000450630.1:n.*467C>T
ENST00000557289.1:c.56-1544C>T	ENSP00000451115.1:n.56-1544C>T
NM_013382.5:c.801C>T , LRG_844t1:c.801C>T	NP_037514.2:p.Asp267=
XM_011536675.1:c.801C>T	XP_011534977.1:p.Asp267=
XM_011536676.1:c.468C>T	XP_011534978.1:p.Asp156=
XM_011536677.1:c.547+3587C>T	XP_011534979.1:n.547+3587C>T
XM_011536678.1:c.801C>T	XP_011534980.1:p.Asp267=
XM_011536679.1:c.-90-1544C>T	XP_011534981.1:n.-90-1544C>T
XM_011536680.1:c.801C>T	XP_011534982.1:p.Asp267=
XR_943416.1:n.1004C>T
XM_011536675.2:c.801C>T	XP_011534977.1:p.Asp267=
XM_011536676.2:c.468C>T	XP_011534978.1:p.Asp156=
XM_011536677.3:c.547+3587C>T	XP_011534979.1:n.547+3587C>T
XR_001750279.1:n.1001C>T
XR_001750282.1:n.1005C>T
XR_943416.3:n.1002C>T
NM_013382.6:c.801C>T	NP_037514.2:p.Asp267=
NM_013382.7:c.801C>T MANE Select	NP_037514.2:p.Asp267=