Canonical Allele Identifier: CA400201422

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48265985T>A (hg19) ; chr17:g.50188624T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50188624T>A , CM000679.2:g.50188624T>A	GRCh38
NC_000017.10:g.48265985T>A , CM000679.1:g.48265985T>A	GRCh37
NC_000017.9:g.45620984T>A	NCBI36
NG_007400.1:g.18016A>T , LRG_1:g.18016A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.3113A>T MANE Select	ENSP00000225964.6:p.Glu1038Val
ENST00000225964.9:c.3113A>T	ENSP00000225964.5:p.Glu1038Val
ENST00000511732.1:n.57A>T
NM_000088.3:c.3113A>T , LRG_1t1:c.3113A>T	NP_000079.2:p.Glu1038Val
XM_005257058.3:c.2843A>T	XP_005257115.2:p.Glu948Val
XM_005257059.3:c.2195A>T	XP_005257116.2:p.Glu732Val
XM_011524341.1:c.2915A>T	XP_011522643.1:p.Glu972Val
XM_005257058.4:c.2843A>T	XP_005257115.2:p.Glu948Val
XM_005257059.4:c.2195A>T	XP_005257116.2:p.Glu732Val
NM_000088.4:c.3113A>T MANE Select	NP_000079.2:p.Glu1038Val