Canonical Allele Identifier: CA400190019

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48262899T>A (hg19) ; chr17:g.50185538T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185538T>A , CM000679.2:g.50185538T>A	GRCh38
NC_000017.10:g.48262899T>A , CM000679.1:g.48262899T>A	GRCh37
NC_000017.9:g.45617898T>A	NCBI36
NG_007400.1:g.21102A>T , LRG_1:g.21102A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4359A>T MANE Select	ENSP00000225964.6:p.Glu1453Asp
ENST00000225964.9:c.4359A>T	ENSP00000225964.5:p.Glu1453Asp
NM_000088.3:c.4359A>T , LRG_1t1:c.4359A>T	NP_000079.2:p.Glu1453Asp
XM_005257058.3:c.4089A>T	XP_005257115.2:p.Glu1363Asp
XM_005257059.3:c.3441A>T	XP_005257116.2:p.Glu1147Asp
XM_011524341.1:c.4161A>T	XP_011522643.1:p.Glu1387Asp
XM_005257058.4:c.4089A>T	XP_005257115.2:p.Glu1363Asp
XM_005257059.4:c.3441A>T	XP_005257116.2:p.Glu1147Asp
NM_000088.4:c.4359A>T MANE Select	NP_000079.2:p.Glu1453Asp