Canonical Allele Identifier: CA500851547

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48274373T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50197012T>G , CM000679.2:g.50197012T>G	GRCh38
NC_000017.10:g.48274373T>G , CM000679.1:g.48274373T>G	GRCh37
NC_000017.9:g.45629372T>G	NCBI36
NG_007400.1:g.9628A>C , LRG_1:g.9628A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000225964.10:c.802A>C MANE Select	ENSP00000225964.6:p.Arg268=
ENST00000225964.9:c.802A>C	ENSP00000225964.5:p.Arg268=
ENST00000495677.1:n.529A>C
NM_000088.3:c.802A>C , LRG_1t1:c.802A>C	NP_000079.2:p.Arg268=
XM_005257058.3:c.802A>C	XP_005257115.2:p.Arg268=
XM_005257059.3:c.802A>C	XP_005257116.2:p.Arg268=
XM_011524341.1:c.802A>C	XP_011522643.1:p.Arg268=
XM_005257058.4:c.802A>C	XP_005257115.2:p.Arg268=
XM_005257059.4:c.802A>C	XP_005257116.2:p.Arg268=
NM_000088.4:c.802A>C MANE Select	NP_000079.2:p.Arg268=