Canonical Allele Identifier: CA400214847
Community Standard Title: NM_000088.4(COL1A1):c.1832G>A (p.Gly611Asp)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192840C>T , CM000679.2:g.50192840C>T GRCh38
NC_000017.10:g.48270201C>T , CM000679.1:g.48270201C>T GRCh37
NC_000017.9:g.45625200C>T NCBI36
NG_007400.1:g.13800G>A , LRG_1:g.13800G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.1832G>A MANE Select NP_000079.2:p.Gly611Asp
ENST00000225964.10:c.1832G>A MANE Select ENSP00000225964.6:p.Gly611Asp
NM_000088.3:c.1832G>A , LRG_1t1:c.1832G>A NP_000079.2:p.Gly611Asp
ENST00000225964.9:c.1832G>A ENSP00000225964.5:p.Gly611Asp
ENST00000476387.1:n.181G>A
XM_005257058.3:c.1832G>A XP_005257115.2:p.Gly611Asp
XM_005257058.4:c.1832G>A XP_005257115.2:p.Gly611Asp
XM_005257059.3:c.958-147G>A XP_005257116.2:n.958-147G>A
XM_005257059.4:c.958-147G>A XP_005257116.2:n.958-147G>A
XM_011524341.1:c.1634G>A XP_011522643.1:p.Gly545Asp