Canonical Allele Identifier: CA4890717

Gene: COL22A1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138636757C>T , CM000670.2:g.138636757C>T	GRCh38
NC_000008.10:g.139649000C>T , CM000670.1:g.139649000C>T	GRCh37
NC_000008.9:g.139718182C>T	NCBI36
NG_054761.1:g.282331G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303045.11:c.3540G>A MANE Select	ENSP00000303153.6:p.Gly1180=
ENST00000303045.10:c.3540G>A	ENSP00000303153.6:p.Gly1180=
ENST00000341807.8:n.1225G>A
ENST00000435777.2:c.2619G>A	ENSP00000387655.2:p.Gly873=
NM_152888.2:c.3540G>A	NP_690848.1:p.Gly1180=
XM_011516883.1:c.3480G>A	XP_011515185.1:p.Gly1160=
XM_011516884.1:c.3441G>A	XP_011515186.1:p.Gly1147=
XM_011516885.1:c.3426G>A	XP_011515187.1:p.Gly1142=
XM_011516886.1:c.3393G>A	XP_011515188.1:p.Gly1131=
XM_011516887.1:c.2454G>A	XP_011515189.1:p.Gly818=
XM_011516888.1:c.3480G>A	XP_011515190.1:p.Gly1160=
XM_011516889.1:c.1836G>A	XP_011515191.1:p.Gly612=
XM_011516890.1:c.1707G>A	XP_011515192.1:p.Gly569=
XM_011516883.2:c.3480G>A	XP_011515185.1:p.Gly1160=
XM_011516884.2:c.3441G>A	XP_011515186.1:p.Gly1147=
XM_011516885.2:c.3426G>A	XP_011515187.1:p.Gly1142=
XM_011516886.3:c.3393G>A	XP_011515188.1:p.Gly1131=
XM_011516887.2:c.2454G>A	XP_011515189.1:p.Gly818=
XM_011516888.2:c.3480G>A	XP_011515190.1:p.Gly1160=
XM_011516889.2:c.1836G>A	XP_011515191.1:p.Gly612=
XM_017013150.2:c.3354G>A	XP_016868639.1:p.Gly1118=
XM_017013151.1:c.3318G>A	XP_016868640.1:p.Gly1106=
XM_017013152.1:c.2454G>A	XP_016868641.1:p.Gly818=
NM_152888.3:c.3540G>A MANE Select	NP_690848.1:p.Gly1180=