Canonical Allele Identifier: CA500991705

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48263244A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185883A>C , CM000679.2:g.50185883A>C	GRCh38
NC_000017.10:g.48263244A>C , CM000679.1:g.48263244A>C	GRCh37
NC_000017.9:g.45618243A>C	NCBI36
NG_007400.1:g.20757T>G , LRG_1:g.20757T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4143T>G MANE Select	ENSP00000225964.6:p.Thr1381=
ENST00000225964.9:c.4143T>G	ENSP00000225964.5:p.Thr1381=
ENST00000510710.3:n.1108T>G
NM_000088.3:c.4143T>G , LRG_1t1:c.4143T>G	NP_000079.2:p.Thr1381=
XM_005257058.3:c.3873T>G	XP_005257115.2:p.Thr1291=
XM_005257059.3:c.3225T>G	XP_005257116.2:p.Thr1075=
XM_011524341.1:c.3945T>G	XP_011522643.1:p.Thr1315=
XM_005257058.4:c.3873T>G	XP_005257115.2:p.Thr1291=
XM_005257059.4:c.3225T>G	XP_005257116.2:p.Thr1075=
NM_000088.4:c.4143T>G MANE Select	NP_000079.2:p.Thr1381=