Canonical Allele Identifier: CA2148330067

Gene: POMT2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77286756G= , CM000676.2:g.77286756G=	GRCh38
NC_000014.8:g.77753099G= , CM000676.1:g.77753099G=	GRCh37
NC_000014.7:g.76822852G=	NCBI36
NG_008897.1:g.39127C= , LRG_844:g.39127C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556394.2:c.861C=	ENSP00000451967.2:p.Thr287=
ENST00000682247.1:c.1320C=	ENSP00000507213.1:p.Thr440=
ENST00000682382.1:c.892C=
ENST00000682395.1:n.1498C=
ENST00000682459.1:n.1023C=
ENST00000682467.1:c.1320C=	ENSP00000508062.1:p.Thr440=
ENST00000682706.1:n.97C=
ENST00000682795.1:c.1320C=	ENSP00000507574.1:p.Thr440=
ENST00000682895.1:n.1036C=
ENST00000682955.1:n.608C=
ENST00000683188.1:c.1295C=
ENST00000683328.1:c.313C=	ENSP00000508096.1:n.313C=
ENST00000683380.1:n.984C=
ENST00000683828.1:c.1029C=
ENST00000684259.1:n.1171C=
ENST00000684444.1:c.67C=
ENST00000684549.1:n.871C=
ENST00000261534.9:c.1320C= MANE Select	ENSP00000261534.4:p.Thr440=
ENST00000261534.8:c.1320C=	ENSP00000261534.4:p.Thr440=
ENST00000452340.7:n.1343C=
ENST00000553880.5:n.191C=
ENST00000554767.5:n.2106C=
ENST00000554884.5:n.312C=
ENST00000556404.1:n.454C=
ENST00000556851.1:n.356C=
ENST00000557675.5:n.410C=
NM_013382.5:c.1320C= , LRG_844t1:c.1320C=	NP_037514.2:p.Thr440=
XM_011536675.1:c.1320C=	XP_011534977.1:p.Thr440=
XM_011536676.1:c.987C=	XP_011534978.1:p.Thr329=
XM_011536677.1:c.861C=	XP_011534979.1:p.Thr287=
XM_011536678.1:c.1320C=	XP_011534980.1:p.Thr440=
XM_011536679.1:c.414C=	XP_011534981.1:p.Thr138=
XR_943416.1:n.1523C=
XM_011536675.2:c.1320C=	XP_011534977.1:p.Thr440=
XM_011536676.2:c.987C=	XP_011534978.1:p.Thr329=
XM_011536677.3:c.861C=	XP_011534979.1:p.Thr287=
XR_001750279.1:n.1520C=
XR_001750282.1:n.1973C=
XR_943416.3:n.1521C=
NM_013382.6:c.1320C=	NP_037514.2:p.Thr440=
NM_013382.7:c.1320C= MANE Select	NP_037514.2:p.Thr440=