Canonical Allele Identifier: CA380179381

Gene: EXT2

Linked Data

• MyVariant Identifiers: chr11:g.44129252T>C (hg19) ; chr11:g.44107702T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44107702T>C , CM000673.2:g.44107702T>C	GRCh38
NC_000011.9:g.44129252T>C , CM000673.1:g.44129252T>C	GRCh37
NC_000011.8:g.44085828T>C	NCBI36
NG_007560.1:g.17154T>C , LRG_494:g.17154T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343631.4:c.-11T>C	ENSP00000342656.3:n.-11T>C
ENST00000395673.8:c.-11T>C	ENSP00000379032.4:n.-11T>C
ENST00000531161.6:n.149T>C
ENST00000682359.1:c.-11T>C	ENSP00000508226.1:n.-11T>C
ENST00000682711.1:c.-544+11850T>C	ENSP00000506803.1:n.-544+11850T>C
ENST00000682815.1:c.-11T>C	ENSP00000507234.1:n.-11T>C
ENST00000682947.1:n.164T>C
ENST00000682993.1:c.-11T>C	ENSP00000507580.1:n.-11T>C
ENST00000683000.1:c.-11T>C	ENSP00000508361.1:n.-11T>C
ENST00000683299.1:n.407T>C
ENST00000683870.1:c.-11T>C	ENSP00000507922.1:n.-11T>C
ENST00000683881.1:n.2551T>C
ENST00000684039.1:c.-11T>C	ENSP00000507677.1:n.-11T>C
ENST00000684124.1:c.-11T>C	ENSP00000508332.1:n.-11T>C
ENST00000684533.1:c.-11T>C	ENSP00000507915.1:n.-11T>C
ENST00000533608.7:c.-11T>C MANE Select	ENSP00000431173.2:n.-11T>C
ENST00000343631.3:c.-11T>C	ENSP00000342656.3:n.-11T>C
ENST00000358681.8:c.-11T>C	ENSP00000351509.4:n.-11T>C
ENST00000395673.7:c.89T>C	ENSP00000379032.3:p.Val30Ala
ENST00000527014.1:c.-11T>C	ENSP00000434716.1:n.-11T>C
ENST00000532479.1:c.-11T>C	ENSP00000433827.1:n.-11T>C
ENST00000533608.5:c.-11T>C	ENSP00000431173.1:n.-11T>C
NM_000401.3:c.89T>C , LRG_494t1:c.89T>C	NP_000392.3:p.Val30Ala
NM_001178083.1:c.-11T>C	NP_001171554.1:n.-11T>C
NM_207122.1:c.-11T>C , LRG_494t2:c.-11T>C	NP_997005.1:n.-11T>C
XM_011519950.1:c.128T>C	XP_011518252.1:p.Val43Ala
XM_011519951.1:c.29T>C	XP_011518253.1:p.Val10Ala
XM_024448383.1:c.128T>C	XP_024304151.1:p.Val43Ala
NM_001178083.2:c.-11T>C	NP_001171554.1:n.-11T>C
NM_207122.2:c.-11T>C MANE Select	NP_997005.1:n.-11T>C
NM_001178083.3:c.-11T>C	NP_001171554.1:n.-11T>C
NM_001389628.1:c.-11T>C	NP_001376557.1:n.-11T>C
NM_001389630.1:c.-11T>C	NP_001376559.1:n.-11T>C