Canonical Allele Identifier: CA2263914178
Community Standard Title: NM_000088.4(COL1A1):c.3897C= (p.Cys1299=)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50186425G= , CM000679.2:g.50186425G= GRCh38
NC_000017.10:g.48263786G= , CM000679.1:g.48263786G= GRCh37
NC_000017.9:g.45618785G= NCBI36
NG_007400.1:g.20215C= , LRG_1:g.20215C=

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.3897C= MANE Select NP_000079.2:p.Cys1299=
ENST00000225964.10:c.3897C= MANE Select ENSP00000225964.6:p.Cys1299=
NM_000088.3:c.3897C= , LRG_1t1:c.3897C= NP_000079.2:p.Cys1299=
ENST00000225964.9:c.3897C= ENSP00000225964.5:p.Cys1299=
ENST00000510710.3:n.566C=
XM_005257058.3:c.3627C= XP_005257115.2:p.Cys1209=
XM_005257058.4:c.3627C= XP_005257115.2:p.Cys1209=
XM_005257059.3:c.2979C= XP_005257116.2:p.Cys993=
XM_005257059.4:c.2979C= XP_005257116.2:p.Cys993=
XM_011524341.1:c.3699C= XP_011522643.1:p.Cys1233=