Canonical Allele Identifier: CA2839103383

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18785682_18785683insCCA , CM000681.2:g.18785682_18785683insCCA	GRCh38
NC_000019.9:g.18896492_18896493insCCA , CM000681.1:g.18896492_18896493insCCA	GRCh37
NC_000019.8:g.18757492_18757493insCCA	NCBI36
NG_007070.1:g.10622_10623insTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1658_1659insTGG MANE Select	ENSP00000222271.2:p.Val553_Leu554insGly
ENST00000222271.6:c.1658_1659insTGG	ENSP00000222271.2:p.Val553_Leu554insGly
ENST00000425807.1:c.1499_1500insTGG	ENSP00000403792.1:p.Val500_Leu501insGly
ENST00000542601.6:c.1559_1560insTGG	ENSP00000439156.2:p.Val520_Leu521insGly
NM_000095.2:c.1658_1659insTGG	NP_000086.2:p.Val553_Leu554insGly
NM_000095.3:c.1658_1659insTGG MANE Select	NP_000086.2:p.Val553_Leu554insGly