Canonical Allele Identifier: CA2263913597
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185407G= , CM000679.2:g.50185407G= GRCh38
NC_000017.10:g.48262768G= , CM000679.1:g.48262768G= GRCh37
NC_000017.9:g.45617767G= NCBI36
NG_007400.1:g.21233C= , LRG_1:g.21233C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.*95C= MANE Select ENSP00000225964.6:n.*95C=
ENST00000225964.9:c.*95C= ENSP00000225964.5:n.*95C=
NM_000088.3:c.*95C= , LRG_1t1:c.*95C= NP_000079.2:n.*95C=
XM_005257058.3:c.*95C= XP_005257115.2:n.*95C=
XM_005257059.3:c.*95C= XP_005257116.2:n.*95C=
XM_011524341.1:c.*95C= XP_011522643.1:n.*95C=
XM_005257058.4:c.*95C= XP_005257115.2:n.*95C=
XM_005257059.4:c.*95C= XP_005257116.2:n.*95C=
NM_000088.4:c.*95C= MANE Select NP_000079.2:n.*95C=