Canonical Allele Identifier: CA2574803767

Gene: EXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44124752_44124753del , CM000673.2:g.44124752_44124753del	GRCh38
NC_000011.9:g.44146302_44146303del , CM000673.1:g.44146302_44146303del	GRCh37
NC_000011.8:g.44102878_44102879del	NCBI36
NG_007560.1:g.34204_34205del , LRG_494:g.34204_34205del

Transcript Alleles

HGVS	Amino-acid change
ENST00000343631.4:c.744-37_744-36del	ENSP00000342656.3:n.744-37_744-36del
ENST00000395673.8:c.744-37_744-36del	ENSP00000379032.4:n.744-37_744-36del
ENST00000531161.6:n.903-37_903-36del
ENST00000682359.1:c.744-37_744-36del	ENSP00000508226.1:n.744-37_744-36del
ENST00000682711.1:c.-544+28900_-544+28901del	ENSP00000506803.1:n.-544+28900_-544+28901...
ENST00000682815.1:c.744-37_744-36del	ENSP00000507234.1:n.744-37_744-36del
ENST00000682947.1:n.918-37_918-36del
ENST00000682993.1:c.744-37_744-36del	ENSP00000507580.1:n.744-37_744-36del
ENST00000683000.1:c.744-37_744-36del	ENSP00000508361.1:n.744-37_744-36del
ENST00000683299.1:n.1161-37_1161-36del
ENST00000683870.1:c.744-37_744-36del	ENSP00000507922.1:n.744-37_744-36del
ENST00000683881.1:n.3305-37_3305-36del
ENST00000684039.1:c.744-37_744-36del	ENSP00000507677.1:n.744-37_744-36del
ENST00000684124.1:c.744-37_744-36del	ENSP00000508332.1:n.744-37_744-36del
ENST00000684533.1:c.744-5293_744-5292del	ENSP00000507915.1:n.744-5293_744-5292del
ENST00000533608.7:c.744-37_744-36del MANE Select	ENSP00000431173.2:n.744-37_744-36del
ENST00000343631.3:c.744-37_744-36del	ENSP00000342656.3:n.744-37_744-36del
ENST00000358681.8:c.744-37_744-36del	ENSP00000351509.4:n.744-37_744-36del
ENST00000395673.7:c.843-37_843-36del	ENSP00000379032.3:n.843-37_843-36del
ENST00000533608.5:c.744-37_744-36del	ENSP00000431173.1:n.744-37_744-36del
NM_000401.3:c.843-37_843-36del , LRG_494t1:c.843-37_843-36del	NP_000392.3:n.843-37_843-36del
NM_001178083.1:c.744-37_744-36del	NP_001171554.1:n.744-37_744-36del
NM_207122.1:c.744-37_744-36del , LRG_494t2:c.744-37_744-36del	NP_997005.1:n.744-37_744-36del
XM_011519950.1:c.882-37_882-36del	XP_011518252.1:n.882-37_882-36del
XM_011519951.1:c.783-37_783-36del	XP_011518253.1:n.783-37_783-36del
XM_024448383.1:c.882-37_882-36del	XP_024304151.1:n.882-37_882-36del
NM_001178083.2:c.744-37_744-36del	NP_001171554.1:n.744-37_744-36del
NM_207122.2:c.744-37_744-36del MANE Select	NP_997005.1:n.744-37_744-36del
NM_001178083.3:c.744-37_744-36del	NP_001171554.1:n.744-37_744-36del
NM_001389628.1:c.744-37_744-36del	NP_001376557.1:n.744-37_744-36del
NM_001389630.1:c.744-37_744-36del	NP_001376559.1:n.744-37_744-36del