Canonical Allele Identifier: CA400227464

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48276662A>T (hg19) ; chr17:g.50199301A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50199301A>T , CM000679.2:g.50199301A>T	GRCh38
NC_000017.10:g.48276662A>T , CM000679.1:g.48276662A>T	GRCh37
NC_000017.9:g.45631661A>T	NCBI36
NG_007400.1:g.7339T>A , LRG_1:g.7339T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.396T>A MANE Select	ENSP00000225964.6:p.Asp132Glu
ENST00000225964.9:c.396T>A	ENSP00000225964.5:p.Asp132Glu
ENST00000474644.1:n.617T>A
ENST00000507689.1:c.450T>A	ENSP00000460459.1:p.Asp150Glu
NM_000088.3:c.396T>A , LRG_1t1:c.396T>A	NP_000079.2:p.Asp132Glu
XM_005257058.3:c.396T>A	XP_005257115.2:p.Asp132Glu
XM_005257059.3:c.396T>A	XP_005257116.2:p.Asp132Glu
XM_011524341.1:c.396T>A	XP_011522643.1:p.Asp132Glu
XM_005257058.4:c.396T>A	XP_005257115.2:p.Asp132Glu
XM_005257059.4:c.396T>A	XP_005257116.2:p.Asp132Glu
NM_000088.4:c.396T>A MANE Select	NP_000079.2:p.Asp132Glu