Canonical Allele Identifier: CA2638704553
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185690G>T , CM000679.2:g.50185690G>T GRCh38
NC_000017.10:g.48263051G>T , CM000679.1:g.48263051G>T GRCh37
NC_000017.9:g.45618050G>T NCBI36
NG_007400.1:g.20950C>A , LRG_1:g.20950C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4249-42C>A MANE Select ENSP00000225964.6:n.4249-42C>A
ENST00000225964.9:c.4249-42C>A ENSP00000225964.5:n.4249-42C>A
NM_000088.3:c.4249-42C>A , LRG_1t1:c.4249-42C>A NP_000079.2:n.4249-42C>A
XM_005257058.3:c.3979-42C>A XP_005257115.2:n.3979-42C>A
XM_005257059.3:c.3331-42C>A XP_005257116.2:n.3331-42C>A
XM_011524341.1:c.4051-42C>A XP_011522643.1:n.4051-42C>A
XM_005257058.4:c.3979-42C>A XP_005257115.2:n.3979-42C>A
XM_005257059.4:c.3331-42C>A XP_005257116.2:n.3331-42C>A
NM_000088.4:c.4249-42C>A MANE Select NP_000079.2:n.4249-42C>A