Canonical Allele Identifier: CA8644306
Community Standard Title: NM_000088.4(COL1A1):c.3979G>A (p.Gly1327Ser)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50186343C>T , CM000679.2:g.50186343C>T GRCh38
NC_000017.10:g.48263704C>T , CM000679.1:g.48263704C>T GRCh37
NC_000017.9:g.45618703C>T NCBI36
NG_007400.1:g.20297G>A , LRG_1:g.20297G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.3979G>A MANE Select NP_000079.2:p.Gly1327Ser
ENST00000225964.10:c.3979G>A MANE Select ENSP00000225964.6:p.Gly1327Ser
NM_000088.3:c.3979G>A , LRG_1t1:c.3979G>A NP_000079.2:p.Gly1327Ser
ENST00000225964.9:c.3979G>A ENSP00000225964.5:p.Gly1327Ser
ENST00000510710.3:n.648G>A
XM_005257058.3:c.3709G>A XP_005257115.2:p.Gly1237Ser
XM_005257058.4:c.3709G>A XP_005257115.2:p.Gly1237Ser
XM_005257059.3:c.3061G>A XP_005257116.2:p.Gly1021Ser
XM_005257059.4:c.3061G>A XP_005257116.2:p.Gly1021Ser
XM_011524341.1:c.3781G>A XP_011522643.1:p.Gly1261Ser