Canonical Allele Identifier: CA291542865
Community Standard Title: NM_000088.4(COL1A1):c.3806G>A (p.Trp1269Ter)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50186648C>T , CM000679.2:g.50186648C>T GRCh38
NC_000017.10:g.48264009C>T , CM000679.1:g.48264009C>T GRCh37
NC_000017.9:g.45619008C>T NCBI36
NG_007400.1:g.19992G>A , LRG_1:g.19992G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.3806G>A MANE Select NP_000079.2:p.Trp1269Ter
ENST00000225964.10:c.3806G>A MANE Select ENSP00000225964.6:p.Trp1269Ter
NM_000088.3:c.3806G>A , LRG_1t1:c.3806G>A NP_000079.2:p.Trp1269Ter
ENST00000225964.9:c.3806G>A ENSP00000225964.5:p.Trp1269Ter
ENST00000510710.3:n.475G>A
XM_005257058.3:c.3536G>A XP_005257115.2:p.Trp1179Ter
XM_005257058.4:c.3536G>A XP_005257115.2:p.Trp1179Ter
XM_005257059.3:c.2888G>A XP_005257116.2:p.Trp963Ter
XM_005257059.4:c.2888G>A XP_005257116.2:p.Trp963Ter
XM_011524341.1:c.3608G>A XP_011522643.1:p.Trp1203Ter