Canonical Allele Identifier: CA2326526628

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787990G= , CM000681.2:g.18787990G=	GRCh38
NC_000019.9:g.18898799G= , CM000681.1:g.18898799G=	GRCh37
NC_000019.8:g.18759799G=	NCBI36
NG_007070.1:g.8316C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.975+222C= MANE Select	ENSP00000222271.2:n.975+222C=
ENST00000222271.6:c.975+222C=	ENSP00000222271.2:n.975+222C=
ENST00000425807.1:c.816+222C=	ENSP00000403792.1:n.816+222C=
ENST00000542601.6:c.876+222C=	ENSP00000439156.2:n.876+222C=
NM_000095.2:c.975+222C=	NP_000086.2:n.975+222C=
NM_000095.3:c.975+222C= MANE Select	NP_000086.2:n.975+222C=