Canonical Allele Identifier: CA500852198

Gene: COL1A1

Linked Data

• gnomAD v4: 17-50199298-G-T
• MyVariant Identifiers: chr17:g.48276659G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50199298G>T , CM000679.2:g.50199298G>T	GRCh38
NC_000017.10:g.48276659G>T , CM000679.1:g.48276659G>T	GRCh37
NC_000017.9:g.45631658G>T	NCBI36
NG_007400.1:g.7342C>A , LRG_1:g.7342C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.399C>A MANE Select	ENSP00000225964.6:p.Gly133=
ENST00000225964.9:c.399C>A	ENSP00000225964.5:p.Gly133=
ENST00000474644.1:n.620C>A
ENST00000507689.1:c.453C>A	ENSP00000460459.1:p.Gly151=
NM_000088.3:c.399C>A , LRG_1t1:c.399C>A	NP_000079.2:p.Gly133=
XM_005257058.3:c.399C>A	XP_005257115.2:p.Gly133=
XM_005257059.3:c.399C>A	XP_005257116.2:p.Gly133=
XM_011524341.1:c.399C>A	XP_011522643.1:p.Gly133=
XM_005257058.4:c.399C>A	XP_005257115.2:p.Gly133=
XM_005257059.4:c.399C>A	XP_005257116.2:p.Gly133=
NM_000088.4:c.399C>A MANE Select	NP_000079.2:p.Gly133=