Canonical Allele Identifier: CA404882998

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18896559A>G (hg19) ; chr19:g.18785749A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785749A>G , CM000681.2:g.18785749A>G	GRCh38
NC_000019.9:g.18896559A>G , CM000681.1:g.18896559A>G	GRCh37
NC_000019.8:g.18757559A>G	NCBI36
NG_007070.1:g.10556T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1592T>C MANE Select	ENSP00000222271.2:p.Phe531Ser
ENST00000222271.6:c.1592T>C	ENSP00000222271.2:p.Phe531Ser
ENST00000425807.1:c.1433T>C	ENSP00000403792.1:p.Phe478Ser
ENST00000542601.6:c.1493T>C	ENSP00000439156.2:p.Phe498Ser
NM_000095.2:c.1592T>C	NP_000086.2:p.Phe531Ser
NM_000095.3:c.1592T>C MANE Select	NP_000086.2:p.Phe531Ser