Canonical Allele Identifier: CA400191281

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48263152A>T (hg19) ; chr17:g.50185791A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185791A>T , CM000679.2:g.50185791A>T	GRCh38
NC_000017.10:g.48263152A>T , CM000679.1:g.48263152A>T	GRCh37
NC_000017.9:g.45618151A>T	NCBI36
NG_007400.1:g.20849T>A , LRG_1:g.20849T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4235T>A MANE Select	ENSP00000225964.6:p.Val1412Asp
ENST00000225964.9:c.4235T>A	ENSP00000225964.5:p.Val1412Asp
NM_000088.3:c.4235T>A , LRG_1t1:c.4235T>A	NP_000079.2:p.Val1412Asp
XM_005257058.3:c.3965T>A	XP_005257115.2:p.Val1322Asp
XM_005257059.3:c.3317T>A	XP_005257116.2:p.Val1106Asp
XM_011524341.1:c.4037T>A	XP_011522643.1:p.Val1346Asp
XM_005257058.4:c.3965T>A	XP_005257115.2:p.Val1322Asp
XM_005257059.4:c.3317T>A	XP_005257116.2:p.Val1106Asp
NM_000088.4:c.4235T>A MANE Select	NP_000079.2:p.Val1412Asp