Canonical Allele Identifier: CA400190321

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48262930G>C (hg19) ; chr17:g.50185569G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185569G>C , CM000679.2:g.50185569G>C	GRCh38
NC_000017.10:g.48262930G>C , CM000679.1:g.48262930G>C	GRCh37
NC_000017.9:g.45617929G>C	NCBI36
NG_007400.1:g.21071C>G , LRG_1:g.21071C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4328C>G MANE Select	ENSP00000225964.6:p.Ala1443Gly
ENST00000225964.9:c.4328C>G	ENSP00000225964.5:p.Ala1443Gly
NM_000088.3:c.4328C>G , LRG_1t1:c.4328C>G	NP_000079.2:p.Ala1443Gly
XM_005257058.3:c.4058C>G	XP_005257115.2:p.Ala1353Gly
XM_005257059.3:c.3410C>G	XP_005257116.2:p.Ala1137Gly
XM_011524341.1:c.4130C>G	XP_011522643.1:p.Ala1377Gly
XM_005257058.4:c.4058C>G	XP_005257115.2:p.Ala1353Gly
XM_005257059.4:c.3410C>G	XP_005257116.2:p.Ala1137Gly
NM_000088.4:c.4328C>G MANE Select	NP_000079.2:p.Ala1443Gly