Canonical Allele Identifier: CA2638710238
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194344dup , CM000679.2:g.50194344dup GRCh38
NC_000017.10:g.48271705dup , CM000679.1:g.48271705dup GRCh37
NC_000017.9:g.45626704dup NCBI36
NG_007400.1:g.12297dup , LRG_1:g.12297dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1614+6dup MANE Select ENSP00000225964.6:n.1614+6dup
ENST00000225964.9:c.1614+6dup ENSP00000225964.5:n.1614+6dup
ENST00000463440.1:n.4+6dup
ENST00000471344.1:n.558+6dup
NM_000088.3:c.1614+6dup , LRG_1t1:c.1614+6dup NP_000079.2:n.1614+6dup
XM_005257058.3:c.1614+6dup XP_005257115.2:n.1614+6dup
XM_005257059.3:c.958-1650dup XP_005257116.2:n.958-1650dup
XM_011524341.1:c.1416+6dup XP_011522643.1:n.1416+6dup
XM_005257058.4:c.1614+6dup XP_005257115.2:n.1614+6dup
XM_005257059.4:c.958-1650dup XP_005257116.2:n.958-1650dup
NM_000088.4:c.1614+6dup MANE Select NP_000079.2:n.1614+6dup