Canonical Allele Identifier: CA1140237992

Gene: COL24A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.86022231C= , CM000663.2:g.86022231C=	GRCh38
NC_000001.10:g.86487914C= , CM000663.1:g.86487914C=	GRCh37
NC_000001.9:g.86260502C=	NCBI36
NG_053093.1:g.139806G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370571.7:c.2256+9G= MANE Select	ENSP00000359603.2:n.2256+9G=
ENST00000370571.6:c.2256+9G=	ENSP00000359603.2:n.2256+9G=
ENST00000426639.5:c.2256+9G=	ENSP00000409515.1:n.2256+9G=
NM_152890.5:c.2256+9G=	NP_690850.2:n.2256+9G=
XM_011541190.1:c.2256+9G=	XP_011539492.1:n.2256+9G=
XM_011541191.1:c.2256+9G=	XP_011539493.1:n.2256+9G=
XM_011541192.1:c.156+9G=	XP_011539494.1:n.156+9G=
NM_001349955.1:c.156+9G=	NP_001336884.1:n.156+9G=
NM_152890.6:c.2256+9G=	NP_690850.2:n.2256+9G=
NR_146340.1:n.2475+9G=
NR_146341.1:n.2544+9G=
NR_146342.1:n.2548+9G=
NR_146343.1:n.2331+9G=
NR_146344.1:n.2331+9G=
NR_146345.1:n.2331+9G=
XM_017000924.2:c.2256+9G=	XP_016856413.1:n.2256+9G=
XM_017000925.2:c.2256+9G=	XP_016856414.1:n.2256+9G=
XM_017000926.1:c.2256+9G=	XP_016856415.1:n.2256+9G=
XM_017000927.1:c.2256+9G=	XP_016856416.1:n.2256+9G=
XM_017000930.1:c.2256+9G=	XP_016856419.1:n.2256+9G=
XR_001737092.1:n.2623+9G=
NM_152890.7:c.2256+9G= MANE Select	NP_690850.2:n.2256+9G=
NR_146340.2:n.2423+9G=
NR_146341.2:n.2620+9G=
NR_146342.2:n.2624+9G=