Canonical Allele Identifier: CA400189939

Gene: COL1A1

Linked Data

• ClinVar Variation Id: 2825583
• ClinVar RCV Id: RCV003631810
• MyVariant Identifiers: chr17:g.48262891A>C (hg19) ; chr17:g.50185530A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185530A>C , CM000679.2:g.50185530A>C	GRCh38
NC_000017.10:g.48262891A>C , CM000679.1:g.48262891A>C	GRCh37
NC_000017.9:g.45617890A>C	NCBI36
NG_007400.1:g.21110T>G , LRG_1:g.21110T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4367T>G MANE Select	ENSP00000225964.6:p.Phe1456Cys
ENST00000225964.9:c.4367T>G	ENSP00000225964.5:p.Phe1456Cys
NM_000088.3:c.4367T>G , LRG_1t1:c.4367T>G	NP_000079.2:p.Phe1456Cys
XM_005257058.3:c.4097T>G	XP_005257115.2:p.Phe1366Cys
XM_005257059.3:c.3449T>G	XP_005257116.2:p.Phe1150Cys
XM_011524341.1:c.4169T>G	XP_011522643.1:p.Phe1390Cys
XM_005257058.4:c.4097T>G	XP_005257115.2:p.Phe1366Cys
XM_005257059.4:c.3449T>G	XP_005257116.2:p.Phe1150Cys
NM_000088.4:c.4367T>G MANE Select	NP_000079.2:p.Phe1456Cys