Canonical Allele Identifier: CA2263920682

Gene: COL1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50199380C= , CM000679.2:g.50199380C=	GRCh38
NC_000017.10:g.48276741C= , CM000679.1:g.48276741C=	GRCh37
NC_000017.9:g.45631740C=	NCBI36
NG_007400.1:g.7260G= , LRG_1:g.7260G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.369+38G= MANE Select	ENSP00000225964.6:n.369+38G=
ENST00000225964.9:c.369+38G=	ENSP00000225964.5:n.369+38G=
ENST00000474644.1:n.590+38G=
ENST00000507689.1:c.423+38G=	ENSP00000460459.1:n.423+38G=
NM_000088.3:c.369+38G= , LRG_1t1:c.369+38G=	NP_000079.2:n.369+38G=
XM_005257058.3:c.369+38G=	XP_005257115.2:n.369+38G=
XM_005257059.3:c.369+38G=	XP_005257116.2:n.369+38G=
XM_011524341.1:c.369+38G=	XP_011522643.1:n.369+38G=
XM_005257058.4:c.369+38G=	XP_005257115.2:n.369+38G=
XM_005257059.4:c.369+38G=	XP_005257116.2:n.369+38G=
NM_000088.4:c.369+38G= MANE Select	NP_000079.2:n.369+38G=