Canonical Allele Identifier: CA1813956598

Gene: EXT1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117835238A= , CM000670.2:g.117835238A=	GRCh38
NC_000008.10:g.118847477A= , CM000670.1:g.118847477A=	GRCh37
NC_000008.9:g.118916658A=	NCBI36
NG_007455.2:g.281582T= , LRG_493:g.281582T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684189.1:n.631+206T=
ENST00000378204.7:c.1164+206T= MANE Select	ENSP00000367446.3:n.1164+206T=
ENST00000436216.2:c.532+206T=
ENST00000378204.6:c.1164+206T=	ENSP00000367446.2:n.1164+206T=
ENST00000436216.1:c.532+206T=
ENST00000437196.1:c.*55+206T=	ENSP00000407299.1:n.*55+206T=
NM_000127.2:c.1164+206T= , LRG_493t1:c.1164+206T=	NP_000118.2:n.1164+206T=
NM_000127.3:c.1164+206T= MANE Select	NP_000118.2:n.1164+206T=