Canonical Allele Identifier: CA291542851
Community Standard Title: NM_000088.4(COL1A1):c.3897C>G (p.Cys1299Trp)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50186425G>C , CM000679.2:g.50186425G>C GRCh38
NC_000017.10:g.48263786G>C , CM000679.1:g.48263786G>C GRCh37
NC_000017.9:g.45618785G>C NCBI36
NG_007400.1:g.20215C>G , LRG_1:g.20215C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.3897C>G MANE Select NP_000079.2:p.Cys1299Trp
ENST00000225964.10:c.3897C>G MANE Select ENSP00000225964.6:p.Cys1299Trp
NM_000088.3:c.3897C>G , LRG_1t1:c.3897C>G NP_000079.2:p.Cys1299Trp
ENST00000225964.9:c.3897C>G ENSP00000225964.5:p.Cys1299Trp
ENST00000510710.3:n.566C>G
XM_005257058.3:c.3627C>G XP_005257115.2:p.Cys1209Trp
XM_005257058.4:c.3627C>G XP_005257115.2:p.Cys1209Trp
XM_005257059.3:c.2979C>G XP_005257116.2:p.Cys993Trp
XM_005257059.4:c.2979C>G XP_005257116.2:p.Cys993Trp
XM_011524341.1:c.3699C>G XP_011522643.1:p.Cys1233Trp