Canonical Allele Identifier: CA400197302
Community Standard Title: NM_000088.4(COL1A1):c.3668T>A (p.Val1223Glu)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50186786A>T , CM000679.2:g.50186786A>T GRCh38
NC_000017.10:g.48264147A>T , CM000679.1:g.48264147A>T GRCh37
NC_000017.9:g.45619146A>T NCBI36
NG_007400.1:g.19854T>A , LRG_1:g.19854T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.3668T>A MANE Select NP_000079.2:p.Val1223Glu
ENST00000225964.10:c.3668T>A MANE Select ENSP00000225964.6:p.Val1223Glu
NM_000088.3:c.3668T>A , LRG_1t1:c.3668T>A NP_000079.2:p.Val1223Glu
ENST00000225964.9:c.3668T>A ENSP00000225964.5:p.Val1223Glu
ENST00000510710.3:n.337T>A
XM_005257058.3:c.3398T>A XP_005257115.2:p.Val1133Glu
XM_005257058.4:c.3398T>A XP_005257115.2:p.Val1133Glu
XM_005257059.3:c.2750T>A XP_005257116.2:p.Val917Glu
XM_005257059.4:c.2750T>A XP_005257116.2:p.Val917Glu
XM_011524341.1:c.3470T>A XP_011522643.1:p.Val1157Glu