Canonical Allele Identifier: CA400200273

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48265503G>C (hg19) ; chr17:g.50188142G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50188142G>C , CM000679.2:g.50188142G>C	GRCh38
NC_000017.10:g.48265503G>C , CM000679.1:g.48265503G>C	GRCh37
NC_000017.9:g.45620502G>C	NCBI36
NG_007400.1:g.18498C>G , LRG_1:g.18498C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.3215C>G MANE Select	ENSP00000225964.6:p.Ala1072Gly
ENST00000225964.9:c.3215C>G	ENSP00000225964.5:p.Ala1072Gly
ENST00000486572.1:n.413C>G
ENST00000511732.1:n.539C>G
NM_000088.3:c.3215C>G , LRG_1t1:c.3215C>G	NP_000079.2:p.Ala1072Gly
XM_005257058.3:c.2945C>G	XP_005257115.2:p.Ala982Gly
XM_005257059.3:c.2297C>G	XP_005257116.2:p.Ala766Gly
XM_011524341.1:c.3017C>G	XP_011522643.1:p.Ala1006Gly
XM_005257058.4:c.2945C>G	XP_005257115.2:p.Ala982Gly
XM_005257059.4:c.2297C>G	XP_005257116.2:p.Ala766Gly
NM_000088.4:c.3215C>G MANE Select	NP_000079.2:p.Ala1072Gly