Canonical Allele Identifier: CA500991722

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48263265C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185904C>G , CM000679.2:g.50185904C>G	GRCh38
NC_000017.10:g.48263265C>G , CM000679.1:g.48263265C>G	GRCh37
NC_000017.9:g.45618264C>G	NCBI36
NG_007400.1:g.20736G>C , LRG_1:g.20736G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4122G>C MANE Select	ENSP00000225964.6:p.Val1374=
ENST00000225964.9:c.4122G>C	ENSP00000225964.5:p.Val1374=
ENST00000510710.3:n.1087G>C
NM_000088.3:c.4122G>C , LRG_1t1:c.4122G>C	NP_000079.2:p.Val1374=
XM_005257058.3:c.3852G>C	XP_005257115.2:p.Val1284=
XM_005257059.3:c.3204G>C	XP_005257116.2:p.Val1068=
XM_011524341.1:c.3924G>C	XP_011522643.1:p.Val1308=
XM_005257058.4:c.3852G>C	XP_005257115.2:p.Val1284=
XM_005257059.4:c.3204G>C	XP_005257116.2:p.Val1068=
NM_000088.4:c.4122G>C MANE Select	NP_000079.2:p.Val1374=