Canonical Allele Identifier: CA2148342592

Gene: POMT2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77301356_77301358delinsCCT , CM000676.2:g.77301356_77301358delinsCCT	GRCh38
NC_000014.8:g.77767699_77767701delinsCCT , CM000676.1:g.77767699_77767701delinsCCT	GRCh37
NC_000014.7:g.76837452_76837454delinsCCT	NCBI36
NG_008897.1:g.24525_24527delinsAGG , LRG_844:g.24525_24527delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553863.6:c.110-109_110-107delinsAGG	ENSP00000508202.1:n.110-109_110-107delinsAGG
ENST00000556394.2:c.358-1797_358-1795delinsAGG	ENSP00000451967.2:n.358-1797_358-1795delinsAGG
ENST00000556880.6:n.681-109_681-107delinsAGG
ENST00000682247.1:c.657-109_657-107delinsAGG	ENSP00000507213.1:n.657-109_657-107delinsAGG
ENST00000682382.1:c.496-2587_496-2585delinsAGG
ENST00000682395.1:n.386-109_386-107delinsAGG
ENST00000682459.1:n.321-109_321-107delinsAGG
ENST00000682467.1:c.657-109_657-107delinsAGG	ENSP00000508062.1:n.657-109_657-107delinsAGG
ENST00000682795.1:c.657-109_657-107delinsAGG	ENSP00000507574.1:n.657-109_657-107delinsAGG
ENST00000682895.1:n.373-109_373-107delinsAGG
ENST00000682955.1:n.212-2587_212-2585delinsAGG
ENST00000683188.1:c.343-1797_343-1795delinsAGG
ENST00000683300.1:c.109+3334_109+3336delinsAGG	ENSP00000507630.1:n.109+3334_109+3336delinsAGG
ENST00000683328.1:c.109+3334_109+3336delinsAGG	ENSP00000508096.1:n.109+3334_109+3336delinsAGG
ENST00000683380.1:n.321-109_321-107delinsAGG
ENST00000683551.1:c.109+1477_109+1479delinsAGG
ENST00000683828.1:c.525+1477_525+1479delinsAGG
ENST00000684259.1:n.508-109_508-107delinsAGG
ENST00000684549.1:n.368-1797_368-1795delinsAGG
ENST00000261534.9:c.657-109_657-107delinsAGG MANE Select	ENSP00000261534.4:n.657-109_657-107delinsAGG
ENST00000261534.8:c.657-109_657-107delinsAGG	ENSP00000261534.4:n.657-109_657-107delinsAGG
ENST00000452340.7:n.680-109_680-107delinsAGG
ENST00000553863.5:n.321-109_321-107delinsAGG
ENST00000554948.1:c.384-109_384-107delinsAGG	ENSP00000452060.1:n.384-109_384-107delinsAGG
ENST00000555675.5:n.373-109_373-107delinsAGG
ENST00000556326.5:c.*323-109_*323-107delinsAGG	ENSP00000450630.1:n.*323-109_*323-107delinsAGG
ENST00000557289.1:c.56-1797_56-1795delinsAGG	ENSP00000451115.1:n.56-1797_56-1795delinsAGG
NM_013382.5:c.657-109_657-107delinsAGG , LRG_844t1:c.657-109_657-107delinsAGG	NP_037514.2:n.657-109_657-107delinsAGG
XM_011536675.1:c.657-109_657-107delinsAGG	XP_011534977.1:n.657-109_657-107delinsAGG
XM_011536676.1:c.324-109_324-107delinsAGG	XP_011534978.1:n.324-109_324-107delinsAGG
XM_011536677.1:c.547+3334_547+3336delinsAGG	XP_011534979.1:n.547+3334_547+3336delinsAGG
XM_011536678.1:c.657-109_657-107delinsAGG	XP_011534980.1:n.657-109_657-107delinsAGG
XM_011536679.1:c.-90-1797_-90-1795delinsAGG	XP_011534981.1:n.-90-1797_-90-1795delinsAGG
XM_011536680.1:c.657-109_657-107delinsAGG	XP_011534982.1:n.657-109_657-107delinsAGG
XR_943416.1:n.860-109_860-107delinsAGG
XM_011536675.2:c.657-109_657-107delinsAGG	XP_011534977.1:n.657-109_657-107delinsAGG
XM_011536676.2:c.324-109_324-107delinsAGG	XP_011534978.1:n.324-109_324-107delinsAGG
XM_011536677.3:c.547+3334_547+3336delinsAGG	XP_011534979.1:n.547+3334_547+3336delinsAGG
XR_001750279.1:n.857-109_857-107delinsAGG
XR_001750282.1:n.861-109_861-107delinsAGG
XR_943416.3:n.858-109_858-107delinsAGG
NM_013382.6:c.657-109_657-107delinsAGG	NP_037514.2:n.657-109_657-107delinsAGG
NM_013382.7:c.657-109_657-107delinsAGG MANE Select	NP_037514.2:n.657-109_657-107delinsAGG