Canonical Allele Identifier: CA400219962

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48272983T>C (hg19) ; chr17:g.50195622T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50195622T>C , CM000679.2:g.50195622T>C	GRCh38
NC_000017.10:g.48272983T>C , CM000679.1:g.48272983T>C	GRCh37
NC_000017.9:g.45627982T>C	NCBI36
NG_007400.1:g.11018A>G , LRG_1:g.11018A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1100A>G MANE Select	ENSP00000225964.6:p.Gln367Arg
ENST00000225964.9:c.1100A>G	ENSP00000225964.5:p.Gln367Arg
ENST00000471344.1:n.44A>G
NM_000088.3:c.1100A>G , LRG_1t1:c.1100A>G	NP_000079.2:p.Gln367Arg
XM_005257058.3:c.1100A>G	XP_005257115.2:p.Gln367Arg
XM_005257059.3:c.957+692A>G	XP_005257116.2:n.957+692A>G
XM_011524341.1:c.958-144A>G	XP_011522643.1:n.958-144A>G
XM_005257058.4:c.1100A>G	XP_005257115.2:p.Gln367Arg
XM_005257059.4:c.957+692A>G	XP_005257116.2:n.957+692A>G
NM_000088.4:c.1100A>G MANE Select	NP_000079.2:p.Gln367Arg