Canonical Allele Identifier: CA400215299

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48271343C>A (hg19) ; chr17:g.50193982C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50193982C>A , CM000679.2:g.50193982C>A	GRCh38
NC_000017.10:g.48271343C>A , CM000679.1:g.48271343C>A	GRCh37
NC_000017.9:g.45626342C>A	NCBI36
NG_007400.1:g.12658G>T , LRG_1:g.12658G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000225964.10:c.1728G>T MANE Select	ENSP00000225964.6:p.Gln576His
ENST00000225964.9:c.1728G>T	ENSP00000225964.5:p.Gln576His
ENST00000463440.1:n.118G>T
ENST00000471344.1:n.760G>T
ENST00000476387.1:n.77G>T
NM_000088.3:c.1728G>T , LRG_1t1:c.1728G>T	NP_000079.2:p.Gln576His
XM_005257058.3:c.1728G>T	XP_005257115.2:p.Gln576His
XM_005257059.3:c.958-1289G>T	XP_005257116.2:n.958-1289G>T
XM_011524341.1:c.1530G>T	XP_011522643.1:p.Gln510His
XM_005257058.4:c.1728G>T	XP_005257115.2:p.Gln576His
XM_005257059.4:c.958-1289G>T	XP_005257116.2:n.958-1289G>T
NM_000088.4:c.1728G>T MANE Select	NP_000079.2:p.Gln576His