Canonical Allele Identifier: CA400206081

Gene: COL1A1

Linked Data

• dbSNP Id: rs1906877569
• MyVariant Identifiers: chr17:g.48266892G>T (hg19) ; chr17:g.50189531G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50189531G>T , CM000679.2:g.50189531G>T	GRCh38
NC_000017.10:g.48266892G>T , CM000679.1:g.48266892G>T	GRCh37
NC_000017.9:g.45621891G>T	NCBI36
NG_007400.1:g.17109C>A , LRG_1:g.17109C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000225964.10:c.2675C>A MANE Select	ENSP00000225964.6:p.Ala892Asp
ENST00000225964.9:c.2675C>A	ENSP00000225964.5:p.Ala892Asp
NM_000088.3:c.2675C>A , LRG_1t1:c.2675C>A	NP_000079.2:p.Ala892Asp
XM_005257058.3:c.2667+148C>A	XP_005257115.2:n.2667+148C>A
XM_005257059.3:c.1757C>A	XP_005257116.2:p.Ala586Asp
XM_011524341.1:c.2477C>A	XP_011522643.1:p.Ala826Asp
XM_005257058.4:c.2667+148C>A	XP_005257115.2:n.2667+148C>A
XM_005257059.4:c.1757C>A	XP_005257116.2:p.Ala586Asp
NM_000088.4:c.2675C>A MANE Select	NP_000079.2:p.Ala892Asp