Canonical Allele Identifier: CA400227413

Gene: COL1A1

Linked Data

• ClinVar Variation Id: 2431889
• ClinVar RCV Id: RCV003142472
• gnomAD v4: 17-50199288-G-A
• MyVariant Identifiers: chr17:g.48276649G>A (hg19) ; chr17:g.50199288G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50199288G>A , CM000679.2:g.50199288G>A	GRCh38
NC_000017.10:g.48276649G>A , CM000679.1:g.48276649G>A	GRCh37
NC_000017.9:g.45631648G>A	NCBI36
NG_007400.1:g.7352C>T , LRG_1:g.7352C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.409C>T MANE Select	ENSP00000225964.6:p.Gln137Ter
ENST00000225964.9:c.409C>T	ENSP00000225964.5:p.Gln137Ter
ENST00000474644.1:n.630C>T
NM_000088.3:c.409C>T , LRG_1t1:c.409C>T	NP_000079.2:p.Gln137Ter
XM_005257058.3:c.409C>T	XP_005257115.2:p.Gln137Ter
XM_005257059.3:c.409C>T	XP_005257116.2:p.Gln137Ter
XM_011524341.1:c.409C>T	XP_011522643.1:p.Gln137Ter
XM_005257058.4:c.409C>T	XP_005257115.2:p.Gln137Ter
XM_005257059.4:c.409C>T	XP_005257116.2:p.Gln137Ter
NM_000088.4:c.409C>T MANE Select	NP_000079.2:p.Gln137Ter