Canonical Allele Identifier: CA500844395

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48265921A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50188560A>C , CM000679.2:g.50188560A>C	GRCh38
NC_000017.10:g.48265921A>C , CM000679.1:g.48265921A>C	GRCh37
NC_000017.9:g.45620920A>C	NCBI36
NG_007400.1:g.18080T>G , LRG_1:g.18080T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.3177T>G MANE Select	ENSP00000225964.6:p.Pro1059=
ENST00000225964.9:c.3177T>G	ENSP00000225964.5:p.Pro1059=
ENST00000511732.1:n.121T>G
NM_000088.3:c.3177T>G , LRG_1t1:c.3177T>G	NP_000079.2:p.Pro1059=
XM_005257058.3:c.2907T>G	XP_005257115.2:p.Pro969=
XM_005257059.3:c.2259T>G	XP_005257116.2:p.Pro753=
XM_011524341.1:c.2979T>G	XP_011522643.1:p.Pro993=
XM_005257058.4:c.2907T>G	XP_005257115.2:p.Pro969=
XM_005257059.4:c.2259T>G	XP_005257116.2:p.Pro753=
NM_000088.4:c.3177T>G MANE Select	NP_000079.2:p.Pro1059=