Canonical Allele Identifier: CA400215531

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48271387C>A (hg19) ; chr17:g.50194026C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50194026C>A , CM000679.2:g.50194026C>A	GRCh38
NC_000017.10:g.48271387C>A , CM000679.1:g.48271387C>A	GRCh37
NC_000017.9:g.45626386C>A	NCBI36
NG_007400.1:g.12614G>T , LRG_1:g.12614G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1684G>T MANE Select	ENSP00000225964.6:p.Asp562Tyr
ENST00000225964.9:c.1684G>T	ENSP00000225964.5:p.Asp562Tyr
ENST00000463440.1:n.74G>T
ENST00000471344.1:n.716G>T
ENST00000476387.1:n.33G>T
NM_000088.3:c.1684G>T , LRG_1t1:c.1684G>T	NP_000079.2:p.Asp562Tyr
XM_005257058.3:c.1684G>T	XP_005257115.2:p.Asp562Tyr
XM_005257059.3:c.958-1333G>T	XP_005257116.2:n.958-1333G>T
XM_011524341.1:c.1486G>T	XP_011522643.1:p.Asp496Tyr
XM_005257058.4:c.1684G>T	XP_005257115.2:p.Asp562Tyr
XM_005257059.4:c.958-1333G>T	XP_005257116.2:n.958-1333G>T
NM_000088.4:c.1684G>T MANE Select	NP_000079.2:p.Asp562Tyr