Canonical Allele Identifier: CA2695228442

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787603_18787605del , CM000681.2:g.18787603_18787605del	GRCh38
NC_000019.9:g.18898412_18898414del , CM000681.1:g.18898412_18898414del	GRCh37
NC_000019.8:g.18759412_18759414del	NCBI36
NG_007070.1:g.8703_8705del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1023_1025del MANE Select	ENSP00000222271.2:p.Glu341del
ENST00000222271.6:c.1023_1025del	ENSP00000222271.2:p.Glu341del
ENST00000425807.1:c.864_866del	ENSP00000403792.1:p.Glu288del
ENST00000542601.6:c.924_926del	ENSP00000439156.2:p.Glu308del
NM_000095.2:c.1023_1025del	NP_000086.2:p.Glu341del
NM_000095.3:c.1023_1025del MANE Select	NP_000086.2:p.Glu341del