Canonical Allele Identifier: CA291542767

Gene: COL1A1

Linked Data

• dbSNP Id: rs1800220
• MyVariant Identifiers: chr17:g.48262958T>A (hg19) ; chr17:g.50185597T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185597T>A , CM000679.2:g.50185597T>A	GRCh38
NC_000017.10:g.48262958T>A , CM000679.1:g.48262958T>A	GRCh37
NC_000017.9:g.45617957T>A	NCBI36
NG_007400.1:g.21043A>T , LRG_1:g.21043A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4300A>T MANE Select	ENSP00000225964.6:p.Thr1434Ser
ENST00000225964.9:c.4300A>T	ENSP00000225964.5:p.Thr1434Ser
NM_000088.3:c.4300A>T , LRG_1t1:c.4300A>T	NP_000079.2:p.Thr1434Ser
XM_005257058.3:c.4030A>T	XP_005257115.2:p.Thr1344Ser
XM_005257059.3:c.3382A>T	XP_005257116.2:p.Thr1128Ser
XM_011524341.1:c.4102A>T	XP_011522643.1:p.Thr1368Ser
XM_005257058.4:c.4030A>T	XP_005257115.2:p.Thr1344Ser
XM_005257059.4:c.3382A>T	XP_005257116.2:p.Thr1128Ser
NM_000088.4:c.4300A>T MANE Select	NP_000079.2:p.Thr1434Ser