Canonical Allele Identifier: CA400190180

Gene: COL1A1

Linked Data

• dbSNP Id: rs1906422062
• COSMIC: COSM4886875
• MyVariant Identifiers: chr17:g.48262912G>T (hg19) ; chr17:g.50185551G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185551G>T , CM000679.2:g.50185551G>T	GRCh38
NC_000017.10:g.48262912G>T , CM000679.1:g.48262912G>T	GRCh37
NC_000017.9:g.45617911G>T	NCBI36
NG_007400.1:g.21089C>A , LRG_1:g.21089C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4346C>A MANE Select	ENSP00000225964.6:p.Ala1449Asp
ENST00000225964.9:c.4346C>A	ENSP00000225964.5:p.Ala1449Asp
NM_000088.3:c.4346C>A , LRG_1t1:c.4346C>A	NP_000079.2:p.Ala1449Asp
XM_005257058.3:c.4076C>A	XP_005257115.2:p.Ala1359Asp
XM_005257059.3:c.3428C>A	XP_005257116.2:p.Ala1143Asp
XM_011524341.1:c.4148C>A	XP_011522643.1:p.Ala1383Asp
XM_005257058.4:c.4076C>A	XP_005257115.2:p.Ala1359Asp
XM_005257059.4:c.3428C>A	XP_005257116.2:p.Ala1143Asp
NM_000088.4:c.4346C>A MANE Select	NP_000079.2:p.Ala1449Asp