Canonical Allele Identifier: CA2809770998
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199392C>A , CM000679.2:g.50199392C>A GRCh38
NC_000017.10:g.48276753C>A , CM000679.1:g.48276753C>A GRCh37
NC_000017.9:g.45631752C>A NCBI36
NG_007400.1:g.7248G>T , LRG_1:g.7248G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.369+26G>T MANE Select ENSP00000225964.6:n.369+26G>T
ENST00000225964.9:c.369+26G>T ENSP00000225964.5:n.369+26G>T
ENST00000474644.1:n.590+26G>T
ENST00000507689.1:c.423+26G>T ENSP00000460459.1:n.423+26G>T
NM_000088.3:c.369+26G>T , LRG_1t1:c.369+26G>T NP_000079.2:n.369+26G>T
XM_005257058.3:c.369+26G>T XP_005257115.2:n.369+26G>T
XM_005257059.3:c.369+26G>T XP_005257116.2:n.369+26G>T
XM_011524341.1:c.369+26G>T XP_011522643.1:n.369+26G>T
XM_005257058.4:c.369+26G>T XP_005257115.2:n.369+26G>T
XM_005257059.4:c.369+26G>T XP_005257116.2:n.369+26G>T
NM_000088.4:c.369+26G>T MANE Select NP_000079.2:n.369+26G>T