Canonical Allele Identifier: CA1967883474

Gene: EXT2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44126824_44126837delinsTTTCTGTGTGGTTC , CM000673.2:g.44126824_44126837delinsTTTCTGTGTGGTTC	GRCh38
NC_000011.9:g.44148374_44148387delinsTTTCTGTGTGGTTC , CM000673.1:g.44148374_44148387delinsTTTCTGTGTGGTTC	GRCh37
NC_000011.8:g.44104950_44104963delinsTTTCTGTGTGGTTC	NCBI36
NG_007560.1:g.36276_36289delinsTTTCTGTGTGGTTC , LRG_494:g.36276_36289delinsTTTCTGTGTGGTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343631.4:c.948_961delinsTTTCTGTGTGGTTC	ENSP00000342656.3:p.Thr316=
ENST00000395673.8:c.948_961delinsTTTCTGTGTGGTTC	ENSP00000379032.4:p.Thr316=
ENST00000531161.6:n.1107_1120delinsTTTCTGTGTGGTTC
ENST00000682359.1:c.939+1840_939+1853delinsTTTCTGTGTGGTTC	ENSP00000508226.1:n.939+1840_939+1853delinsTTTCTGTGTGGTTC
ENST00000682711.1:c.-544+30972_-544+30985delinsTTTCTGTGTGGTTC	ENSP00000506803.1:n.-544+30972_-544+30985delinsTTTCTGTGTGGTTC...
ENST00000682815.1:c.948_961delinsTTTCTGTGTGGTTC	ENSP00000507234.1:p.Thr316=
ENST00000682947.1:n.1122_1135delinsTTTCTGTGTGGTTC
ENST00000682993.1:c.948_961delinsTTTCTGTGTGGTTC	ENSP00000507580.1:p.Thr316=
ENST00000683000.1:c.948_961delinsTTTCTGTGTGGTTC	ENSP00000508361.1:p.Thr316=
ENST00000683299.1:n.1365_1378delinsTTTCTGTGTGGTTC
ENST00000683870.1:c.948_961delinsTTTCTGTGTGGTTC	ENSP00000507922.1:p.Thr316=
ENST00000683881.1:n.3509_3522delinsTTTCTGTGTGGTTC
ENST00000684039.1:c.948_961delinsTTTCTGTGTGGTTC	ENSP00000507677.1:p.Thr316=
ENST00000684124.1:c.948_961delinsTTTCTGTGTGGTTC	ENSP00000508332.1:p.Thr316=
ENST00000684533.1:c.744-3221_744-3208delinsTTTCTGTGTGGTTC	ENSP00000507915.1:n.744-3221_744-3208delinsTTTCTGTGTGGTTC
ENST00000533608.7:c.948_961delinsTTTCTGTGTGGTTC MANE Select	ENSP00000431173.2:p.Thr316=
ENST00000343631.3:c.948_961delinsTTTCTGTGTGGTTC	ENSP00000342656.3:p.Thr316=
ENST00000358681.8:c.948_961delinsTTTCTGTGTGGTTC	ENSP00000351509.4:p.Thr316=
ENST00000395673.7:c.1047_1060delinsTTTCTGTGTGGTTC	ENSP00000379032.3:p.Thr349=
ENST00000531161.5:n.125_138delinsTTTCTGTGTGGTTC
ENST00000533608.5:c.948_961delinsTTTCTGTGTGGTTC	ENSP00000431173.1:p.Thr316=
NM_000401.3:c.1047_1060delinsTTTCTGTGTGGTTC , LRG_494t1:c.1047_1060delinsTTTCTGTGTGGTTC	NP_000392.3:p.Thr349=
NM_001178083.1:c.948_961delinsTTTCTGTGTGGTTC	NP_001171554.1:p.Thr316=
NM_207122.1:c.948_961delinsTTTCTGTGTGGTTC , LRG_494t2:c.948_961delinsTTTCTGTGTGGTTC	NP_997005.1:p.Thr316=
XM_011519950.1:c.1086_1099delinsTTTCTGTGTGGTTC	XP_011518252.1:p.Thr362=
XM_011519951.1:c.987_1000delinsTTTCTGTGTGGTTC	XP_011518253.1:p.Thr329=
XM_024448383.1:c.1086_1099delinsTTTCTGTGTGGTTC	XP_024304151.1:p.Thr362=
NM_001178083.2:c.948_961delinsTTTCTGTGTGGTTC	NP_001171554.1:p.Thr316=
NM_207122.2:c.948_961delinsTTTCTGTGTGGTTC MANE Select	NP_997005.1:p.Thr316=
NM_001178083.3:c.948_961delinsTTTCTGTGTGGTTC	NP_001171554.1:p.Thr316=
NM_001389628.1:c.948_961delinsTTTCTGTGTGGTTC	NP_001376557.1:p.Thr316=
NM_001389630.1:c.948_961delinsTTTCTGTGTGGTTC	NP_001376559.1:p.Thr316=