Canonical Allele Identifier: CA2263917601
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192798G= , CM000679.2:g.50192798G= GRCh38
NC_000017.10:g.48270159G= , CM000679.1:g.48270159G= GRCh37
NC_000017.9:g.45625158G= NCBI36
NG_007400.1:g.13842C= , LRG_1:g.13842C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1874C= MANE Select ENSP00000225964.6:p.Ala625=
ENST00000225964.9:c.1874C= ENSP00000225964.5:p.Ala625=
ENST00000476387.1:n.223C=
NM_000088.3:c.1874C= , LRG_1t1:c.1874C= NP_000079.2:p.Ala625=
XM_005257058.3:c.1874C= XP_005257115.2:p.Ala625=
XM_005257059.3:c.958-105C= XP_005257116.2:n.958-105C=
XM_011524341.1:c.1676C= XP_011522643.1:p.Ala559=
XM_005257058.4:c.1874C= XP_005257115.2:p.Ala625=
XM_005257059.4:c.958-105C= XP_005257116.2:n.958-105C=
NM_000088.4:c.1874C= MANE Select NP_000079.2:p.Ala625=