Canonical Allele Identifier: CA2595039414
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50184495_50184498dup , CM000679.2:g.50184495_50184498dup GRCh38
NC_000017.10:g.48261856_48261859dup , CM000679.1:g.48261856_48261859dup GRCh37
NC_000017.9:g.45616855_45616858dup NCBI36
NG_007400.1:g.22145_22148dup , LRG_1:g.22145_22148dup

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.*1007_*1010dup MANE Select ENSP00000225964.6:n.*1007_*1010dup
ENST00000225964.9:c.*1007_*1010dup ENSP00000225964.5:n.*1007_*1010dup
NM_000088.3:c.*1007_*1010dup , LRG_1t1:c.*1007_*1010dup NP_000079.2:n.*1007_*1010dup
XM_005257058.3:c.*1007_*1010dup XP_005257115.2:n.*1007_*1010dup
XM_005257059.3:c.*1007_*1010dup XP_005257116.2:n.*1007_*1010dup
XM_011524341.1:c.*1007_*1010dup XP_011522643.1:n.*1007_*1010dup
XM_005257058.4:c.*1007_*1010dup XP_005257115.2:n.*1007_*1010dup
XM_005257059.4:c.*1007_*1010dup XP_005257116.2:n.*1007_*1010dup
NM_000088.4:c.*1007_*1010dup MANE Select NP_000079.2:n.*1007_*1010dup