Canonical Allele Identifier: CA2148328993

Gene: POMT2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306508_77306512delinsTTCCC , CM000676.2:g.77306508_77306512delinsTTCCC	GRCh38
NC_000014.8:g.77772851_77772855delinsTTCCC , CM000676.1:g.77772851_77772855delinsTTCCC	GRCh37
NC_000014.7:g.76842604_76842608delinsTTCCC	NCBI36
NG_008897.1:g.19371_19375delinsGGGAA , LRG_844:g.19371_19375delinsGGGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556394.2:c.249-1712_249-1708delinsGGGAA	ENSP00000451967.2:n.249-1712_249-1708delinsGGGAA
ENST00000556880.6:n.267-71_267-67delinsGGGAA
ENST00000682247.1:c.334-71_334-67delinsGGGAA	ENSP00000507213.1:n.334-71_334-67delinsGGGAA
ENST00000682382.1:c.282-71_282-67delinsGGGAA
ENST00000682467.1:c.334-71_334-67delinsGGGAA	ENSP00000508062.1:n.334-71_334-67delinsGGGAA
ENST00000682795.1:c.334-71_334-67delinsGGGAA	ENSP00000507574.1:n.334-71_334-67delinsGGGAA
ENST00000683188.1:c.129-71_129-67delinsGGGAA
ENST00000683828.1:c.203-71_203-67delinsGGGAA
ENST00000684066.1:n.29-71_29-67delinsGGGAA
ENST00000684102.1:n.80-71_80-67delinsGGGAA
ENST00000684259.1:n.185-71_185-67delinsGGGAA
ENST00000684600.1:c.148-71_148-67delinsGGGAA
ENST00000684746.1:n.31-71_31-67delinsGGGAA
ENST00000261534.9:c.334-71_334-67delinsGGGAA MANE Select	ENSP00000261534.4:n.334-71_334-67delinsGGGAA
ENST00000261534.8:c.334-71_334-67delinsGGGAA	ENSP00000261534.4:n.334-71_334-67delinsGGGAA
ENST00000452340.7:n.357-71_357-67delinsGGGAA
ENST00000554948.1:c.61-71_61-67delinsGGGAA	ENSP00000452060.1:n.61-71_61-67delinsGGGAA
ENST00000555788.5:n.168-71_168-67delinsGGGAA
ENST00000556326.5:c.249-71_249-67delinsGGGAA	ENSP00000450630.1:n.249-71_249-67delinsGGGAA
ENST00000556880.5:n.267-71_267-67delinsGGGAA
ENST00000557525.1:n.424-71_424-67delinsGGGAA
NM_013382.5:c.334-71_334-67delinsGGGAA , LRG_844t1:c.334-71_334-67delinsGGGAA	NP_037514.2:n.334-71_334-67delinsGGGAA
XM_011536675.1:c.334-71_334-67delinsGGGAA	XP_011534977.1:n.334-71_334-67delinsGGGAA
XM_011536676.1:c.1-71_1-67delinsGGGAA	XP_011534978.1:n.1-71_1-67delinsGGGAA
XM_011536677.1:c.334-71_334-67delinsGGGAA	XP_011534979.1:n.334-71_334-67delinsGGGAA
XM_011536678.1:c.334-71_334-67delinsGGGAA	XP_011534980.1:n.334-71_334-67delinsGGGAA
XM_011536680.1:c.334-71_334-67delinsGGGAA	XP_011534982.1:n.334-71_334-67delinsGGGAA
XR_943416.1:n.537-71_537-67delinsGGGAA
XM_011536675.2:c.334-71_334-67delinsGGGAA	XP_011534977.1:n.334-71_334-67delinsGGGAA
XM_011536676.2:c.1-71_1-67delinsGGGAA	XP_011534978.1:n.1-71_1-67delinsGGGAA
XM_011536677.3:c.334-71_334-67delinsGGGAA	XP_011534979.1:n.334-71_334-67delinsGGGAA
XR_001750279.1:n.534-71_534-67delinsGGGAA
XR_001750282.1:n.538-71_538-67delinsGGGAA
XR_943416.3:n.535-71_535-67delinsGGGAA
NM_013382.6:c.334-71_334-67delinsGGGAA	NP_037514.2:n.334-71_334-67delinsGGGAA
NM_013382.7:c.334-71_334-67delinsGGGAA MANE Select	NP_037514.2:n.334-71_334-67delinsGGGAA