Canonical Allele Identifier: CA291547382

Gene: COL1A1

Linked Data

• ClinVar Variation Id: 425640
• ClinVar RCV Id: RCV000490675
• dbSNP Id: rs72645337
• gnomAD v4: 17-50196624-C-G
• MyVariant Identifiers: chr17:g.48273985C>G (hg19) ; chr17:g.50196624C>G (hg38)
• PubMed: PMID:25944380

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50196624C>G , CM000679.2:g.50196624C>G	GRCh38
NC_000017.10:g.48273985C>G , CM000679.1:g.48273985C>G	GRCh37
NC_000017.9:g.45628984C>G	NCBI36
NG_007400.1:g.10016G>C , LRG_1:g.10016G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.851G>C MANE Select	ENSP00000225964.6:p.Gly284Ala
ENST00000225964.9:c.851G>C	ENSP00000225964.5:p.Gly284Ala
ENST00000495677.1:n.578G>C
NM_000088.3:c.851G>C , LRG_1t1:c.851G>C	NP_000079.2:p.Gly284Ala
XM_005257058.3:c.851G>C	XP_005257115.2:p.Gly284Ala
XM_005257059.3:c.851G>C	XP_005257116.2:p.Gly284Ala
XM_011524341.1:c.851G>C	XP_011522643.1:p.Gly284Ala
XM_005257058.4:c.851G>C	XP_005257115.2:p.Gly284Ala
XM_005257059.4:c.851G>C	XP_005257116.2:p.Gly284Ala
NM_000088.4:c.851G>C MANE Select	NP_000079.2:p.Gly284Ala