Canonical Allele Identifier: CA2580094367
Community Standard Title: NM_000088.4(COL1A1):c.588+5G>A
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50198156C>T , CM000679.2:g.50198156C>T GRCh38
NC_000017.10:g.48275517C>T , CM000679.1:g.48275517C>T GRCh37
NC_000017.9:g.45630516C>T NCBI36
NG_007400.1:g.8484G>A , LRG_1:g.8484G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.588+5G>A MANE Select NP_000079.2:n.588+5G>A
ENST00000225964.10:c.588+5G>A MANE Select ENSP00000225964.6:n.588+5G>A
NM_000088.3:c.588+5G>A , LRG_1t1:c.588+5G>A NP_000079.2:n.588+5G>A
ENST00000225964.9:c.588+5G>A ENSP00000225964.5:n.588+5G>A
ENST00000495677.1:n.315+5G>A
XM_005257058.3:c.588+5G>A XP_005257115.2:n.588+5G>A
XM_005257058.4:c.588+5G>A XP_005257115.2:n.588+5G>A
XM_005257059.3:c.588+5G>A XP_005257116.2:n.588+5G>A
XM_005257059.4:c.588+5G>A XP_005257116.2:n.588+5G>A
XM_011524341.1:c.588+5G>A XP_011522643.1:n.588+5G>A