Canonical Allele Identifier: CA291547129
Community Standard Title: NM_000088.4(COL1A1):c.992C>T (p.Ala331Val)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196165G>A , CM000679.2:g.50196165G>A GRCh38
NC_000017.10:g.48273526G>A , CM000679.1:g.48273526G>A GRCh37
NC_000017.9:g.45628525G>A NCBI36
NG_007400.1:g.10475C>T , LRG_1:g.10475C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.992C>T MANE Select NP_000079.2:p.Ala331Val
ENST00000225964.10:c.992C>T MANE Select ENSP00000225964.6:p.Ala331Val
NM_000088.3:c.992C>T , LRG_1t1:c.992C>T NP_000079.2:p.Ala331Val
ENST00000225964.9:c.992C>T ENSP00000225964.5:p.Ala331Val
ENST00000485870.1:n.317C>T
XM_005257058.3:c.992C>T XP_005257115.2:p.Ala331Val
XM_005257058.4:c.992C>T XP_005257115.2:p.Ala331Val
XM_005257059.3:c.957+149C>T XP_005257116.2:n.957+149C>T
XM_005257059.4:c.957+149C>T XP_005257116.2:n.957+149C>T
XM_011524341.1:c.957+149C>T XP_011522643.1:n.957+149C>T