Canonical Allele Identifier: CA2148327535

Gene: POMT2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77278568A= , CM000676.2:g.77278568A=	GRCh38
NC_000014.8:g.77744911A= , CM000676.1:g.77744911A=	GRCh37
NC_000014.7:g.76814664A=	NCBI36
NG_008897.1:g.47315T= , LRG_844:g.47315T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555134.2:n.958-60T=
ENST00000556394.2:c.1574-60T=	ENSP00000451967.2:n.1574-60T=
ENST00000682247.1:c.2022-60T=	ENSP00000507213.1:n.2022-60T=
ENST00000682395.1:n.2497-60T=
ENST00000682459.1:n.1736-60T=
ENST00000682467.1:c.1892-60T=	ENSP00000508062.1:n.1892-60T=
ENST00000682795.1:c.2180-60T=	ENSP00000507574.1:n.2180-60T=
ENST00000682895.1:n.1749-60T=
ENST00000682955.1:n.1607-60T=
ENST00000683188.1:c.2294-60T=
ENST00000683380.1:n.1697-60T=
ENST00000683907.1:c.298-60T=	ENSP00000507754.1:n.298-60T=
ENST00000684259.1:n.3800-60T=
ENST00000684538.1:n.1412-60T=
ENST00000684549.1:n.1584-60T=
ENST00000261534.9:c.2033-60T= MANE Select	ENSP00000261534.4:n.2033-60T=
ENST00000261534.8:c.2033-60T=	ENSP00000261534.4:n.2033-60T=
ENST00000452340.7:n.3009-60T=
ENST00000554767.5:n.2819-60T=
ENST00000555710.1:c.394-60T=	ENSP00000451730.1:n.394-60T=
ENST00000556394.1:c.88-60T=
ENST00000556446.1:n.334-60T=
ENST00000602717.5:c.248-60T=	ENSP00000487704.1:n.248-60T=
NM_013382.5:c.2033-60T= , LRG_844t1:c.2033-60T=	NP_037514.2:n.2033-60T=
XM_011536675.1:c.2222-60T=	XP_011534977.1:n.2222-60T=
XM_011536676.1:c.1889-60T=	XP_011534978.1:n.1889-60T=
XM_011536677.1:c.1763-60T=	XP_011534979.1:n.1763-60T=
XM_011536679.1:c.1316-60T=	XP_011534981.1:n.1316-60T=
XR_943416.1:n.2286-60T=
XM_011536675.2:c.2222-60T=	XP_011534977.1:n.2222-60T=
XM_011536676.2:c.1889-60T=	XP_011534978.1:n.1889-60T=
XM_011536677.3:c.1763-60T=	XP_011534979.1:n.1763-60T=
XR_001750279.1:n.2319-60T=
XR_001750282.1:n.2972-60T=
XR_943416.3:n.2284-60T=
NM_013382.6:c.2033-60T=	NP_037514.2:n.2033-60T=
NM_013382.7:c.2033-60T= MANE Select	NP_037514.2:n.2033-60T=