Canonical Allele Identifier: CA500991363

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48262932C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185571C>G , CM000679.2:g.50185571C>G	GRCh38
NC_000017.10:g.48262932C>G , CM000679.1:g.48262932C>G	GRCh37
NC_000017.9:g.45617931C>G	NCBI36
NG_007400.1:g.21069G>C , LRG_1:g.21069G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4326G>C MANE Select	ENSP00000225964.6:p.Val1442=
ENST00000225964.9:c.4326G>C	ENSP00000225964.5:p.Val1442=
NM_000088.3:c.4326G>C , LRG_1t1:c.4326G>C	NP_000079.2:p.Val1442=
XM_005257058.3:c.4056G>C	XP_005257115.2:p.Val1352=
XM_005257059.3:c.3408G>C	XP_005257116.2:p.Val1136=
XM_011524341.1:c.4128G>C	XP_011522643.1:p.Val1376=
XM_005257058.4:c.4056G>C	XP_005257115.2:p.Val1352=
XM_005257059.4:c.3408G>C	XP_005257116.2:p.Val1136=
NM_000088.4:c.4326G>C MANE Select	NP_000079.2:p.Val1442=