Canonical Allele Identifier: CA400221323

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48273536T>A (hg19) ; chr17:g.50196175T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50196175T>A , CM000679.2:g.50196175T>A	GRCh38
NC_000017.10:g.48273536T>A , CM000679.1:g.48273536T>A	GRCh37
NC_000017.9:g.45628535T>A	NCBI36
NG_007400.1:g.10465A>T , LRG_1:g.10465A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.982A>T MANE Select	ENSP00000225964.6:p.Thr328Ser
ENST00000225964.9:c.982A>T	ENSP00000225964.5:p.Thr328Ser
ENST00000485870.1:n.307A>T
NM_000088.3:c.982A>T , LRG_1t1:c.982A>T	NP_000079.2:p.Thr328Ser
XM_005257058.3:c.982A>T	XP_005257115.2:p.Thr328Ser
XM_005257059.3:c.957+139A>T	XP_005257116.2:n.957+139A>T
XM_011524341.1:c.957+139A>T	XP_011522643.1:n.957+139A>T
XM_005257058.4:c.982A>T	XP_005257115.2:p.Thr328Ser
XM_005257059.4:c.957+139A>T	XP_005257116.2:n.957+139A>T
NM_000088.4:c.982A>T MANE Select	NP_000079.2:p.Thr328Ser