Canonical Allele Identifier: CA2613200677

Gene: EXT2

Linked Data

• gnomAD v4: 11-44107568-A-ATCTCG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44107568_44107569insTCTCG , CM000673.2:g.44107568_44107569insTCTCG	GRCh38
NC_000011.9:g.44129118_44129119insTCTCG , CM000673.1:g.44129118_44129119insTCTCG	GRCh37
NC_000011.8:g.44085694_44085695insTCTCG	NCBI36
NG_007560.1:g.17020_17021insTCTCG , LRG_494:g.17020_17021insTCTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343631.4:c.-30-115_-30-114insTCTCG	ENSP00000342656.3:n.-30-115_-30-114insTCTCG
ENST00000395673.8:c.-30-115_-30-114insTCTCG	ENSP00000379032.4:n.-30-115_-30-114insTCTCG
ENST00000531161.6:n.130-115_130-114insTCTCG
ENST00000682359.1:c.-30-115_-30-114insTCTCG	ENSP00000508226.1:n.-30-115_-30-114insTCTCG
ENST00000682711.1:c.-544+11716_-544+11717insTCTCG	ENSP00000506803.1:n.-544+11716_-544+11717insTCTCG
ENST00000682815.1:c.-30-115_-30-114insTCTCG	ENSP00000507234.1:n.-30-115_-30-114insTCTCG
ENST00000682947.1:n.145-115_145-114insTCTCG
ENST00000682993.1:c.-30-115_-30-114insTCTCG	ENSP00000507580.1:n.-30-115_-30-114insTCTCG
ENST00000683000.1:c.-30-115_-30-114insTCTCG	ENSP00000508361.1:n.-30-115_-30-114insTCTCG
ENST00000683299.1:n.273_274insTCTCG
ENST00000683870.1:c.-30-115_-30-114insTCTCG	ENSP00000507922.1:n.-30-115_-30-114insTCTCG
ENST00000683881.1:n.2532-115_2532-114insTCTCG
ENST00000684039.1:c.-30-115_-30-114insTCTCG	ENSP00000507677.1:n.-30-115_-30-114insTCTCG
ENST00000684124.1:c.-30-115_-30-114insTCTCG	ENSP00000508332.1:n.-30-115_-30-114insTCTCG
ENST00000684533.1:c.-30-115_-30-114insTCTCG	ENSP00000507915.1:n.-30-115_-30-114insTCTCG
ENST00000533608.7:c.-30-115_-30-114insTCTCG MANE Select	ENSP00000431173.2:n.-30-115_-30-114insTCTCG
ENST00000343631.3:c.-30-115_-30-114insTCTCG	ENSP00000342656.3:n.-30-115_-30-114insTCTCG
ENST00000358681.8:c.-30-115_-30-114insTCTCG	ENSP00000351509.4:n.-30-115_-30-114insTCTCG
ENST00000395673.7:c.70-115_70-114insTCTCG	ENSP00000379032.3:n.70-115_70-114insTCTCG
ENST00000527014.1:c.-30-115_-30-114insTCTCG	ENSP00000434716.1:n.-30-115_-30-114insTCTCG
ENST00000532479.1:c.-30-115_-30-114insTCTCG	ENSP00000433827.1:n.-30-115_-30-114insTCTCG
ENST00000533608.5:c.-30-115_-30-114insTCTCG	ENSP00000431173.1:n.-30-115_-30-114insTCTCG
NM_000401.3:c.70-115_70-114insTCTCG , LRG_494t1:c.70-115_70-114insTCTCG	NP_000392.3:n.70-115_70-114insTCTCG
NM_001178083.1:c.-30-115_-30-114insTCTCG	NP_001171554.1:n.-30-115_-30-114insTCTCG
NM_207122.1:c.-30-115_-30-114insTCTCG , LRG_494t2:c.-30-115_-30-114insTCTCG	NP_997005.1:n.-30-115_-30-114insTCTCG
XM_011519950.1:c.109-115_109-114insTCTCG	XP_011518252.1:n.109-115_109-114insTCTCG
XM_011519951.1:c.10-115_10-114insTCTCG	XP_011518253.1:n.10-115_10-114insTCTCG
XM_024448383.1:c.109-115_109-114insTCTCG	XP_024304151.1:n.109-115_109-114insTCTCG
NM_001178083.2:c.-30-115_-30-114insTCTCG	NP_001171554.1:n.-30-115_-30-114insTCTCG
NM_207122.2:c.-30-115_-30-114insTCTCG MANE Select	NP_997005.1:n.-30-115_-30-114insTCTCG
NM_001178083.3:c.-30-115_-30-114insTCTCG	NP_001171554.1:n.-30-115_-30-114insTCTCG
NM_001389628.1:c.-30-115_-30-114insTCTCG	NP_001376557.1:n.-30-115_-30-114insTCTCG
NM_001389630.1:c.-30-115_-30-114insTCTCG	NP_001376559.1:n.-30-115_-30-114insTCTCG