Canonical Allele Identifier: CA500848321

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48270382T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50193021T>G , CM000679.2:g.50193021T>G	GRCh38
NC_000017.10:g.48270382T>G , CM000679.1:g.48270382T>G	GRCh37
NC_000017.9:g.45625381T>G	NCBI36
NG_007400.1:g.13619A>C , LRG_1:g.13619A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1794A>C MANE Select	ENSP00000225964.6:p.Arg598=
ENST00000225964.9:c.1794A>C	ENSP00000225964.5:p.Arg598=
ENST00000476387.1:n.143A>C
NM_000088.3:c.1794A>C , LRG_1t1:c.1794A>C	NP_000079.2:p.Arg598=
XM_005257058.3:c.1794A>C	XP_005257115.2:p.Arg598=
XM_005257059.3:c.958-328A>C	XP_005257116.2:n.958-328A>C
XM_011524341.1:c.1596A>C	XP_011522643.1:p.Arg532=
XM_005257058.4:c.1794A>C	XP_005257115.2:p.Arg598=
XM_005257059.4:c.958-328A>C	XP_005257116.2:n.958-328A>C
NM_000088.4:c.1794A>C MANE Select	NP_000079.2:p.Arg598=