Canonical Allele Identifier: CA2263920287
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50198460G= , CM000679.2:g.50198460G= GRCh38
NC_000017.10:g.48275821G= , CM000679.1:g.48275821G= GRCh37
NC_000017.9:g.45630820G= NCBI36
NG_007400.1:g.8180C= , LRG_1:g.8180C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.516C= MANE Select ENSP00000225964.6:p.Thr172=
ENST00000225964.9:c.516C= ENSP00000225964.5:p.Thr172=
ENST00000495677.1:n.243C=
NM_000088.3:c.516C= , LRG_1t1:c.516C= NP_000079.2:p.Thr172=
XM_005257058.3:c.516C= XP_005257115.2:p.Thr172=
XM_005257059.3:c.516C= XP_005257116.2:p.Thr172=
XM_011524341.1:c.516C= XP_011522643.1:p.Thr172=
XM_005257058.4:c.516C= XP_005257115.2:p.Thr172=
XM_005257059.4:c.516C= XP_005257116.2:p.Thr172=
NM_000088.4:c.516C= MANE Select NP_000079.2:p.Thr172=