Canonical Allele Identifier: CA2638680355
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50198660C>T , CM000679.2:g.50198660C>T GRCh38
NC_000017.10:g.48276021C>T , CM000679.1:g.48276021C>T GRCh37
NC_000017.9:g.45631020C>T NCBI36
NG_007400.1:g.7980G>A , LRG_1:g.7980G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.472-156G>A MANE Select ENSP00000225964.6:n.472-156G>A
ENST00000225964.9:c.472-156G>A ENSP00000225964.5:n.472-156G>A
ENST00000495677.1:n.43G>A
NM_000088.3:c.472-156G>A , LRG_1t1:c.472-156G>A NP_000079.2:n.472-156G>A
XM_005257058.3:c.472-156G>A XP_005257115.2:n.472-156G>A
XM_005257059.3:c.472-156G>A XP_005257116.2:n.472-156G>A
XM_011524341.1:c.472-156G>A XP_011522643.1:n.472-156G>A
XM_005257058.4:c.472-156G>A XP_005257115.2:n.472-156G>A
XM_005257059.4:c.472-156G>A XP_005257116.2:n.472-156G>A
NM_000088.4:c.472-156G>A MANE Select NP_000079.2:n.472-156G>A