Canonical Allele Identifier: CA500844428
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48265954A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188593A>T , CM000679.2:g.50188593A>T GRCh38
NC_000017.10:g.48265954A>T , CM000679.1:g.48265954A>T GRCh37
NC_000017.9:g.45620953A>T NCBI36
NG_007400.1:g.18047T>A , LRG_1:g.18047T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.3144T>A MANE Select ENSP00000225964.6:p.Pro1048=
ENST00000225964.9:c.3144T>A ENSP00000225964.5:p.Pro1048=
ENST00000511732.1:n.88T>A
NM_000088.3:c.3144T>A , LRG_1t1:c.3144T>A NP_000079.2:p.Pro1048=
XM_005257058.3:c.2874T>A XP_005257115.2:p.Pro958=
XM_005257059.3:c.2226T>A XP_005257116.2:p.Pro742=
XM_011524341.1:c.2946T>A XP_011522643.1:p.Pro982=
XM_005257058.4:c.2874T>A XP_005257115.2:p.Pro958=
XM_005257059.4:c.2226T>A XP_005257116.2:p.Pro742=
NM_000088.4:c.3144T>A MANE Select NP_000079.2:p.Pro1048=