Canonical Allele Identifier: CA8645516

Gene: COL1A1

Linked Data

• dbSNP Id: rs199507352
• ExAC: 17:48273929 G / T
• gnomAD v2: 17-48273929-G-T
• gnomAD v3: 17-50196568-G-T
• gnomAD v4: 17-50196568-G-T
• MyVariant Identifiers: chr17:g.48273929G>T (hg19) ; chr17:g.50196568G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50196568G>T , CM000679.2:g.50196568G>T	GRCh38
NC_000017.10:g.48273929G>T , CM000679.1:g.48273929G>T	GRCh37
NC_000017.9:g.45628928G>T	NCBI36
NG_007400.1:g.10072C>A , LRG_1:g.10072C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.859-40C>A MANE Select	ENSP00000225964.6:n.859-40C>A
ENST00000225964.9:c.859-40C>A	ENSP00000225964.5:n.859-40C>A
ENST00000485870.1:n.28C>A
ENST00000495677.1:n.586-40C>A
NM_000088.3:c.859-40C>A , LRG_1t1:c.859-40C>A	NP_000079.2:n.859-40C>A
XM_005257058.3:c.859-40C>A	XP_005257115.2:n.859-40C>A
XM_005257059.3:c.859-40C>A	XP_005257116.2:n.859-40C>A
XM_011524341.1:c.859-40C>A	XP_011522643.1:n.859-40C>A
XM_005257058.4:c.859-40C>A	XP_005257115.2:n.859-40C>A
XM_005257059.4:c.859-40C>A	XP_005257116.2:n.859-40C>A
NM_000088.4:c.859-40C>A MANE Select	NP_000079.2:n.859-40C>A