Canonical Allele Identifier: CA1823893821

Gene: COL22A1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138872266C= , CM000670.2:g.138872266C=	GRCh38
NC_000008.10:g.139884509C= , CM000670.1:g.139884509C=	GRCh37
NC_000008.9:g.139953691C=	NCBI36
NG_054761.1:g.46822G=

Transcript Alleles

HGVS	Amino-acid Change
NM_152888.3:c.658+5484G= MANE Select	NP_690848.1:n.658+5484G=
ENST00000303045.11:c.658+5484G= MANE Select	ENSP00000303153.6:n.658+5484G=
NM_152888.2:c.658+5484G=	NP_690848.1:n.658+5484G=
ENST00000303045.10:c.658+5484G=	ENSP00000303153.6:n.658+5484G=
ENST00000435777.2:c.658+5484G=	ENSP00000387655.2:n.658+5484G=
XM_011516883.1:c.658+5484G=	XP_011515185.1:n.658+5484G=
XM_011516883.2:c.658+5484G=	XP_011515185.1:n.658+5484G=
XM_011516884.1:c.658+5484G=	XP_011515186.1:n.658+5484G=
XM_011516884.2:c.658+5484G=	XP_011515186.1:n.658+5484G=
XM_011516885.1:c.658+5484G=	XP_011515187.1:n.658+5484G=
XM_011516885.2:c.658+5484G=	XP_011515187.1:n.658+5484G=
XM_011516886.1:c.571+5484G=	XP_011515188.1:n.571+5484G=
XM_011516886.3:c.571+5484G=	XP_011515188.1:n.571+5484G=
XM_011516888.1:c.658+5484G=	XP_011515190.1:n.658+5484G=
XM_011516888.2:c.658+5484G=	XP_011515190.1:n.658+5484G=
XM_011516891.1:c.658+5484G=	XP_011515193.1:n.658+5484G=
XM_017013150.2:c.532+5484G=	XP_016868639.1:n.532+5484G=
XM_017013151.1:c.658+5484G=	XP_016868640.1:n.658+5484G=
XR_001745487.1:n.1199+5484G=