Canonical Allele Identifier: CA2695200280
Community Standard Title: NM_000088.4(COL1A1):c.1516-5A>G
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194452T>C , CM000679.2:g.50194452T>C GRCh38
NC_000017.10:g.48271813T>C , CM000679.1:g.48271813T>C GRCh37
NC_000017.9:g.45626812T>C NCBI36
NG_007400.1:g.12188A>G , LRG_1:g.12188A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.1516-5A>G MANE Select NP_000079.2:n.1516-5A>G
ENST00000225964.10:c.1516-5A>G MANE Select ENSP00000225964.6:n.1516-5A>G
NM_000088.3:c.1516-5A>G , LRG_1t1:c.1516-5A>G NP_000079.2:n.1516-5A>G
ENST00000225964.9:c.1516-5A>G ENSP00000225964.5:n.1516-5A>G
ENST00000471344.1:n.460-5A>G
XM_005257058.3:c.1516-5A>G XP_005257115.2:n.1516-5A>G
XM_005257058.4:c.1516-5A>G XP_005257115.2:n.1516-5A>G
XM_005257059.3:c.958-1759A>G XP_005257116.2:n.958-1759A>G
XM_005257059.4:c.958-1759A>G XP_005257116.2:n.958-1759A>G
XM_011524341.1:c.1318-5A>G XP_011522643.1:n.1318-5A>G