Canonical Allele Identifier: CA500849857
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48272097T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194736T>A , CM000679.2:g.50194736T>A GRCh38
NC_000017.10:g.48272097T>A , CM000679.1:g.48272097T>A GRCh37
NC_000017.9:g.45627096T>A NCBI36
NG_007400.1:g.11904A>T , LRG_1:g.11904A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1446A>T MANE Select ENSP00000225964.6:p.Gly482=
ENST00000225964.9:c.1446A>T ENSP00000225964.5:p.Gly482=
ENST00000471344.1:n.390A>T
NM_000088.3:c.1446A>T , LRG_1t1:c.1446A>T NP_000079.2:p.Gly482=
XM_005257058.3:c.1446A>T XP_005257115.2:p.Gly482=
XM_005257059.3:c.957+1578A>T XP_005257116.2:n.957+1578A>T
XM_011524341.1:c.1248A>T XP_011522643.1:p.Gly416=
XM_005257058.4:c.1446A>T XP_005257115.2:p.Gly482=
XM_005257059.4:c.957+1578A>T XP_005257116.2:n.957+1578A>T
NM_000088.4:c.1446A>T MANE Select NP_000079.2:p.Gly482=