Canonical Allele Identifier: CA400200131

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48265483C>G (hg19) ; chr17:g.50188122C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50188122C>G , CM000679.2:g.50188122C>G	GRCh38
NC_000017.10:g.48265483C>G , CM000679.1:g.48265483C>G	GRCh37
NC_000017.9:g.45620482C>G	NCBI36
NG_007400.1:g.18518G>C , LRG_1:g.18518G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.3235G>C MANE Select	ENSP00000225964.6:p.Gly1079Arg
ENST00000225964.9:c.3235G>C	ENSP00000225964.5:p.Gly1079Arg
ENST00000486572.1:n.433G>C
ENST00000511732.1:n.559G>C
NM_000088.3:c.3235G>C , LRG_1t1:c.3235G>C	NP_000079.2:p.Gly1079Arg
XM_005257058.3:c.2965G>C	XP_005257115.2:p.Gly989Arg
XM_005257059.3:c.2317G>C	XP_005257116.2:p.Gly773Arg
XM_011524341.1:c.3037G>C	XP_011522643.1:p.Gly1013Arg
XM_005257058.4:c.2965G>C	XP_005257115.2:p.Gly989Arg
XM_005257059.4:c.2317G>C	XP_005257116.2:p.Gly773Arg
NM_000088.4:c.3235G>C MANE Select	NP_000079.2:p.Gly1079Arg