Canonical Allele Identifier: CA2638710176
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194117dup , CM000679.2:g.50194117dup GRCh38
NC_000017.10:g.48271478dup , CM000679.1:g.48271478dup GRCh37
NC_000017.9:g.45626477dup NCBI36
NG_007400.1:g.12527dup , LRG_1:g.12527dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1668+17dup MANE Select ENSP00000225964.6:n.1668+17dup
ENST00000225964.9:c.1668+17dup ENSP00000225964.5:n.1668+17dup
ENST00000463440.1:n.58+17dup
ENST00000471344.1:n.629dup
NM_000088.3:c.1668+17dup , LRG_1t1:c.1668+17dup NP_000079.2:n.1668+17dup
XM_005257058.3:c.1668+17dup XP_005257115.2:n.1668+17dup
XM_005257059.3:c.958-1420dup XP_005257116.2:n.958-1420dup
XM_011524341.1:c.1470+17dup XP_011522643.1:n.1470+17dup
XM_005257058.4:c.1668+17dup XP_005257115.2:n.1668+17dup
XM_005257059.4:c.958-1420dup XP_005257116.2:n.958-1420dup
NM_000088.4:c.1668+17dup MANE Select NP_000079.2:n.1668+17dup