Canonical Allele Identifier: CA984449691
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50184487_50184494dup , CM000679.2:g.50184487_50184494dup GRCh38
NC_000017.10:g.48261848_48261855dup , CM000679.1:g.48261848_48261855dup GRCh37
NC_000017.9:g.45616847_45616854dup NCBI36
NG_007400.1:g.22157_22164dup , LRG_1:g.22157_22164dup

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.*1019_*1026dup MANE Select ENSP00000225964.6:n.*1019_*1026dup
ENST00000225964.9:c.*1019_*1026dup ENSP00000225964.5:n.*1019_*1026dup
NM_000088.3:c.*1019_*1026dup , LRG_1t1:c.*1019_*1026dup NP_000079.2:n.*1019_*1026dup
XM_005257058.3:c.*1019_*1026dup XP_005257115.2:n.*1019_*1026dup
XM_005257059.3:c.*1019_*1026dup XP_005257116.2:n.*1019_*1026dup
XM_011524341.1:c.*1019_*1026dup XP_011522643.1:n.*1019_*1026dup
XM_005257058.4:c.*1019_*1026dup XP_005257115.2:n.*1019_*1026dup
XM_005257059.4:c.*1019_*1026dup XP_005257116.2:n.*1019_*1026dup
NM_000088.4:c.*1019_*1026dup MANE Select NP_000079.2:n.*1019_*1026dup