Canonical Allele Identifier: CA2809757422
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196566T>G , CM000679.2:g.50196566T>G GRCh38
NC_000017.10:g.48273927T>G , CM000679.1:g.48273927T>G GRCh37
NC_000017.9:g.45628926T>G NCBI36
NG_007400.1:g.10074A>C , LRG_1:g.10074A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.859-38A>C MANE Select ENSP00000225964.6:n.859-38A>C
ENST00000225964.9:c.859-38A>C ENSP00000225964.5:n.859-38A>C
ENST00000485870.1:n.30A>C
ENST00000495677.1:n.586-38A>C
NM_000088.3:c.859-38A>C , LRG_1t1:c.859-38A>C NP_000079.2:n.859-38A>C
XM_005257058.3:c.859-38A>C XP_005257115.2:n.859-38A>C
XM_005257059.3:c.859-38A>C XP_005257116.2:n.859-38A>C
XM_011524341.1:c.859-38A>C XP_011522643.1:n.859-38A>C
XM_005257058.4:c.859-38A>C XP_005257115.2:n.859-38A>C
XM_005257059.4:c.859-38A>C XP_005257116.2:n.859-38A>C
NM_000088.4:c.859-38A>C MANE Select NP_000079.2:n.859-38A>C