Canonical Allele Identifier: CA404882684

Gene: COMP

Linked Data

• MyVariant Identifiers: chr19:g.18896538A>C (hg19) ; chr19:g.18785728A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785728A>C , CM000681.2:g.18785728A>C	GRCh38
NC_000019.9:g.18896538A>C , CM000681.1:g.18896538A>C	GRCh37
NC_000019.8:g.18757538A>C	NCBI36
NG_007070.1:g.10577T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1613T>G MANE Select	ENSP00000222271.2:p.Val538Gly
ENST00000222271.6:c.1613T>G	ENSP00000222271.2:p.Val538Gly
ENST00000425807.1:c.1454T>G	ENSP00000403792.1:p.Val485Gly
ENST00000542601.6:c.1514T>G	ENSP00000439156.2:p.Val505Gly
NM_000095.2:c.1613T>G	NP_000086.2:p.Val538Gly
NM_000095.3:c.1613T>G MANE Select	NP_000086.2:p.Val538Gly