Canonical Allele Identifier: CA2809757338
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192783T>G , CM000679.2:g.50192783T>G GRCh38
NC_000017.10:g.48270144T>G , CM000679.1:g.48270144T>G GRCh37
NC_000017.9:g.45625143T>G NCBI36
NG_007400.1:g.13857A>C , LRG_1:g.13857A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1875+14A>C MANE Select ENSP00000225964.6:n.1875+14A>C
ENST00000225964.9:c.1875+14A>C ENSP00000225964.5:n.1875+14A>C
ENST00000476387.1:n.224+14A>C
NM_000088.3:c.1875+14A>C , LRG_1t1:c.1875+14A>C NP_000079.2:n.1875+14A>C
XM_005257058.3:c.1875+14A>C XP_005257115.2:n.1875+14A>C
XM_005257059.3:c.958-90A>C XP_005257116.2:n.958-90A>C
XM_011524341.1:c.1677+14A>C XP_011522643.1:n.1677+14A>C
XM_005257058.4:c.1875+14A>C XP_005257115.2:n.1875+14A>C
XM_005257059.4:c.958-90A>C XP_005257116.2:n.958-90A>C
NM_000088.4:c.1875+14A>C MANE Select NP_000079.2:n.1875+14A>C