Canonical Allele Identifier: CA626485667

Gene: COL1A1

Linked Data

• dbSNP Id: rs1285824060
• gnomAD v2: 17-48262342-G-T
• gnomAD v3: 17-50184981-G-T
• gnomAD v4: 17-50184981-G-T
• MyVariant Identifiers: chr17:g.48262342G>T (hg19) ; chr17:g.50184981G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50184981G>T , CM000679.2:g.50184981G>T	GRCh38
NC_000017.10:g.48262342G>T , CM000679.1:g.48262342G>T	GRCh37
NC_000017.9:g.45617341G>T	NCBI36
NG_007400.1:g.21659C>A , LRG_1:g.21659C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.*521C>A MANE Select	ENSP00000225964.6:n.*521C>A
ENST00000225964.9:c.*521C>A	ENSP00000225964.5:n.*521C>A
NM_000088.3:c.*521C>A , LRG_1t1:c.*521C>A	NP_000079.2:n.*521C>A
XM_005257058.3:c.*521C>A	XP_005257115.2:n.*521C>A
XM_005257059.3:c.*521C>A	XP_005257116.2:n.*521C>A
XM_011524341.1:c.*521C>A	XP_011522643.1:n.*521C>A
XM_005257058.4:c.*521C>A	XP_005257115.2:n.*521C>A
XM_005257059.4:c.*521C>A	XP_005257116.2:n.*521C>A
NM_000088.4:c.*521C>A MANE Select	NP_000079.2:n.*521C>A