Canonical Allele Identifier: CA2638710339
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194708C>T , CM000679.2:g.50194708C>T GRCh38
NC_000017.10:g.48272069C>T , CM000679.1:g.48272069C>T GRCh37
NC_000017.9:g.45627068C>T NCBI36
NG_007400.1:g.11932G>A , LRG_1:g.11932G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1461+13G>A MANE Select ENSP00000225964.6:n.1461+13G>A
ENST00000225964.9:c.1461+13G>A ENSP00000225964.5:n.1461+13G>A
ENST00000471344.1:n.405+13G>A
NM_000088.3:c.1461+13G>A , LRG_1t1:c.1461+13G>A NP_000079.2:n.1461+13G>A
XM_005257058.3:c.1461+13G>A XP_005257115.2:n.1461+13G>A
XM_005257059.3:c.957+1606G>A XP_005257116.2:n.957+1606G>A
XM_011524341.1:c.1263+13G>A XP_011522643.1:n.1263+13G>A
XM_005257058.4:c.1461+13G>A XP_005257115.2:n.1461+13G>A
XM_005257059.4:c.957+1606G>A XP_005257116.2:n.957+1606G>A
NM_000088.4:c.1461+13G>A MANE Select NP_000079.2:n.1461+13G>A