Canonical Allele Identifier: CA400191998

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48263254T>C (hg19) ; chr17:g.50185893T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185893T>C , CM000679.2:g.50185893T>C	GRCh38
NC_000017.10:g.48263254T>C , CM000679.1:g.48263254T>C	GRCh37
NC_000017.9:g.45618253T>C	NCBI36
NG_007400.1:g.20747A>G , LRG_1:g.20747A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4133A>G MANE Select	ENSP00000225964.6:p.Asp1378Gly
ENST00000225964.9:c.4133A>G	ENSP00000225964.5:p.Asp1378Gly
ENST00000510710.3:n.1098A>G
NM_000088.3:c.4133A>G , LRG_1t1:c.4133A>G	NP_000079.2:p.Asp1378Gly
XM_005257058.3:c.3863A>G	XP_005257115.2:p.Asp1288Gly
XM_005257059.3:c.3215A>G	XP_005257116.2:p.Asp1072Gly
XM_011524341.1:c.3935A>G	XP_011522643.1:p.Asp1312Gly
XM_005257058.4:c.3863A>G	XP_005257115.2:p.Asp1288Gly
XM_005257059.4:c.3215A>G	XP_005257116.2:p.Asp1072Gly
NM_000088.4:c.4133A>G MANE Select	NP_000079.2:p.Asp1378Gly