Canonical Allele Identifier: CA500851158
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48273314A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195953A>T , CM000679.2:g.50195953A>T GRCh38
NC_000017.10:g.48273314A>T , CM000679.1:g.48273314A>T GRCh37
NC_000017.9:g.45628313A>T NCBI36
NG_007400.1:g.10687T>A , LRG_1:g.10687T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1026T>A MANE Select ENSP00000225964.6:p.Pro342=
ENST00000225964.9:c.1026T>A ENSP00000225964.5:p.Pro342=
NM_000088.3:c.1026T>A , LRG_1t1:c.1026T>A NP_000079.2:p.Pro342=
XM_005257058.3:c.1026T>A XP_005257115.2:p.Pro342=
XM_005257059.3:c.957+361T>A XP_005257116.2:n.957+361T>A
XM_011524341.1:c.957+361T>A XP_011522643.1:n.957+361T>A
XM_005257058.4:c.1026T>A XP_005257115.2:p.Pro342=
XM_005257059.4:c.957+361T>A XP_005257116.2:n.957+361T>A
NM_000088.4:c.1026T>A MANE Select NP_000079.2:p.Pro342=