Canonical Allele Identifier: CA400227471

Gene: COL1A1

Linked Data

• gnomAD v4: 17-50199303-C-A
• MyVariant Identifiers: chr17:g.48276664C>A (hg19) ; chr17:g.50199303C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50199303C>A , CM000679.2:g.50199303C>A	GRCh38
NC_000017.10:g.48276664C>A , CM000679.1:g.48276664C>A	GRCh37
NC_000017.9:g.45631663C>A	NCBI36
NG_007400.1:g.7337G>T , LRG_1:g.7337G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.394G>T MANE Select	ENSP00000225964.6:p.Asp132Tyr
ENST00000225964.9:c.394G>T	ENSP00000225964.5:p.Asp132Tyr
ENST00000474644.1:n.615G>T
ENST00000507689.1:c.448G>T	ENSP00000460459.1:p.Asp150Tyr
NM_000088.3:c.394G>T , LRG_1t1:c.394G>T	NP_000079.2:p.Asp132Tyr
XM_005257058.3:c.394G>T	XP_005257115.2:p.Asp132Tyr
XM_005257059.3:c.394G>T	XP_005257116.2:p.Asp132Tyr
XM_011524341.1:c.394G>T	XP_011522643.1:p.Asp132Tyr
XM_005257058.4:c.394G>T	XP_005257115.2:p.Asp132Tyr
XM_005257059.4:c.394G>T	XP_005257116.2:p.Asp132Tyr
NM_000088.4:c.394G>T MANE Select	NP_000079.2:p.Asp132Tyr