Canonical Allele Identifier: CA2148327591

Gene: POMT2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77278690A= , CM000676.2:g.77278690A=	GRCh38
NC_000014.8:g.77745033A= , CM000676.1:g.77745033A=	GRCh37
NC_000014.7:g.76814786A=	NCBI36
NG_008897.1:g.47193T= , LRG_844:g.47193T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555134.2:n.957+39T=
ENST00000556394.2:c.1573+39T=	ENSP00000451967.2:n.1573+39T=
ENST00000682247.1:c.2021+39T=	ENSP00000507213.1:n.2021+39T=
ENST00000682395.1:n.2496+39T=
ENST00000682459.1:n.1735+39T=
ENST00000682467.1:c.1892-182T=	ENSP00000508062.1:n.1892-182T=
ENST00000682795.1:c.2179+39T=	ENSP00000507574.1:n.2179+39T=
ENST00000682895.1:n.1748+39T=
ENST00000682955.1:n.1606+39T=
ENST00000683188.1:c.2293+39T=
ENST00000683380.1:n.1696+39T=
ENST00000683907.1:c.297+39T=	ENSP00000507754.1:n.297+39T=
ENST00000684259.1:n.3799+39T=
ENST00000684538.1:n.1411+39T=
ENST00000684549.1:n.1583+39T=
ENST00000261534.9:c.2032+39T= MANE Select	ENSP00000261534.4:n.2032+39T=
ENST00000261534.8:c.2032+39T=	ENSP00000261534.4:n.2032+39T=
ENST00000452340.7:n.3008+39T=
ENST00000554767.5:n.2818+39T=
ENST00000555710.1:c.393+39T=	ENSP00000451730.1:n.393+39T=
ENST00000556394.1:c.88-182T=
ENST00000556446.1:n.333+39T=
ENST00000602717.5:c.247+39T=	ENSP00000487704.1:n.247+39T=
NM_013382.5:c.2032+39T= , LRG_844t1:c.2032+39T=	NP_037514.2:n.2032+39T=
XM_011536675.1:c.2221+39T=	XP_011534977.1:n.2221+39T=
XM_011536676.1:c.1888+39T=	XP_011534978.1:n.1888+39T=
XM_011536677.1:c.1762+39T=	XP_011534979.1:n.1762+39T=
XM_011536679.1:c.1315+39T=	XP_011534981.1:n.1315+39T=
XR_943416.1:n.2285+39T=
XM_011536675.2:c.2221+39T=	XP_011534977.1:n.2221+39T=
XM_011536676.2:c.1888+39T=	XP_011534978.1:n.1888+39T=
XM_011536677.3:c.1762+39T=	XP_011534979.1:n.1762+39T=
XR_001750279.1:n.2318+39T=
XR_001750282.1:n.2971+39T=
XR_943416.3:n.2283+39T=
NM_013382.6:c.2032+39T=	NP_037514.2:n.2032+39T=
NM_013382.7:c.2032+39T= MANE Select	NP_037514.2:n.2032+39T=