Canonical Allele Identifier: CA2499220949

Gene: EXT2

Linked Data

• ClinVar Variation Id: 1074447
• ClinVar RCV Id: RCV001387737
• dbSNP Id: rs2134965356

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44107776_44107780del , CM000673.2:g.44107776_44107780del	GRCh38
NC_000011.9:g.44129326_44129330del , CM000673.1:g.44129326_44129330del	GRCh37
NC_000011.8:g.44085902_44085906del	NCBI36
NG_007560.1:g.17228_17232del , LRG_494:g.17228_17232del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343631.4:c.64_68del	ENSP00000342656.3:p.His22AsnfsTer?
ENST00000395673.8:c.64_68del	ENSP00000379032.4:p.His22AsnfsTer?
ENST00000531161.6:n.223_227del
ENST00000682359.1:c.64_68del	ENSP00000508226.1:p.His22AsnfsTer?
ENST00000682711.1:c.-544+11924_-544+11928del	ENSP00000506803.1:n.-544+11924_-544+11928del
ENST00000682815.1:c.64_68del	ENSP00000507234.1:p.His22AsnfsTer?
ENST00000682947.1:n.238_242del
ENST00000682993.1:c.64_68del	ENSP00000507580.1:p.His22AsnfsTer?
ENST00000683000.1:c.64_68del	ENSP00000508361.1:p.His22AsnfsTer?
ENST00000683299.1:n.481_485del
ENST00000683870.1:c.64_68del	ENSP00000507922.1:p.His22AsnfsTer?
ENST00000683881.1:n.2625_2629del
ENST00000684039.1:c.64_68del	ENSP00000507677.1:p.His22AsnfsTer?
ENST00000684124.1:c.64_68del	ENSP00000508332.1:p.His22AsnfsTer?
ENST00000684533.1:c.64_68del	ENSP00000507915.1:p.His22AsnfsTer?
ENST00000533608.7:c.64_68del MANE Select	ENSP00000431173.2:p.His22AsnfsTer?
ENST00000343631.3:c.64_68del	ENSP00000342656.3:p.His22AsnfsTer?
ENST00000358681.8:c.64_68del	ENSP00000351509.4:p.His22AsnfsTer?
ENST00000395673.7:c.163_167del	ENSP00000379032.3:p.His55AsnfsTer?
ENST00000527014.1:c.64_68del	ENSP00000434716.1:p.His22AsnfsTer?
ENST00000532479.1:c.64_68del	ENSP00000433827.1:p.His22AsnfsTer?
ENST00000533608.5:c.64_68del	ENSP00000431173.1:p.His22AsnfsTer?
NM_000401.3:c.163_167del , LRG_494t1:c.163_167del	NP_000392.3:p.His55AsnfsTer?
NM_001178083.1:c.64_68del	NP_001171554.1:p.His22AsnfsTer?
NM_207122.1:c.64_68del , LRG_494t2:c.64_68del	NP_997005.1:p.His22AsnfsTer?
XM_011519950.1:c.202_206del	XP_011518252.1:p.His68AsnfsTer?
XM_011519951.1:c.103_107del	XP_011518253.1:p.His35AsnfsTer?
XM_024448383.1:c.202_206del	XP_024304151.1:p.His68AsnfsTer?
NM_001178083.2:c.64_68del	NP_001171554.1:p.His22AsnfsTer?
NM_207122.2:c.64_68del MANE Select	NP_997005.1:p.His22AsnfsTer?
NM_001178083.3:c.64_68del	NP_001171554.1:p.His22AsnfsTer?
NM_001389628.1:c.64_68del	NP_001376557.1:p.His22AsnfsTer?
NM_001389630.1:c.64_68del	NP_001376559.1:p.His22AsnfsTer?