Canonical Allele Identifier: CA400219930

Gene: COL1A1

Linked Data

• ClinVar Variation Id: 456728
• ClinVar RCV Id: RCV000538665 ; RCV001260276
• dbSNP Id: rs1555574151
• MyVariant Identifiers: chr17:g.48272980C>G (hg19) ; chr17:g.50195619C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50195619C>G , CM000679.2:g.50195619C>G	GRCh38
NC_000017.10:g.48272980C>G , CM000679.1:g.48272980C>G	GRCh37
NC_000017.9:g.45627979C>G	NCBI36
NG_007400.1:g.11021G>C , LRG_1:g.11021G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1103G>C MANE Select	ENSP00000225964.6:p.Gly368Ala
ENST00000225964.9:c.1103G>C	ENSP00000225964.5:p.Gly368Ala
ENST00000471344.1:n.47G>C
NM_000088.3:c.1103G>C , LRG_1t1:c.1103G>C	NP_000079.2:p.Gly368Ala
XM_005257058.3:c.1103G>C	XP_005257115.2:p.Gly368Ala
XM_005257059.3:c.957+695G>C	XP_005257116.2:n.957+695G>C
XM_011524341.1:c.958-141G>C	XP_011522643.1:n.958-141G>C
XM_005257058.4:c.1103G>C	XP_005257115.2:p.Gly368Ala
XM_005257059.4:c.957+695G>C	XP_005257116.2:n.957+695G>C
NM_000088.4:c.1103G>C MANE Select	NP_000079.2:p.Gly368Ala