Canonical Allele Identifier: CA2263913882
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185845T= , CM000679.2:g.50185845T= GRCh38
NC_000017.10:g.48263206T= , CM000679.1:g.48263206T= GRCh37
NC_000017.9:g.45618205T= NCBI36
NG_007400.1:g.20795A= , LRG_1:g.20795A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4181A= MANE Select ENSP00000225964.6:p.Asn1394=
ENST00000225964.9:c.4181A= ENSP00000225964.5:p.Asn1394=
ENST00000510710.3:n.1146A=
NM_000088.3:c.4181A= , LRG_1t1:c.4181A= NP_000079.2:p.Asn1394=
XM_005257058.3:c.3911A= XP_005257115.2:p.Asn1304=
XM_005257059.3:c.3263A= XP_005257116.2:p.Asn1088=
XM_011524341.1:c.3983A= XP_011522643.1:p.Asn1328=
XM_005257058.4:c.3911A= XP_005257115.2:p.Asn1304=
XM_005257059.4:c.3263A= XP_005257116.2:p.Asn1088=
NM_000088.4:c.4181A= MANE Select NP_000079.2:p.Asn1394=