Canonical Allele Identifier: CA400193156
Community Standard Title: NM_000088.4(COL1A1):c.3975G>T (p.Trp1325Cys)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50186347C>A , CM000679.2:g.50186347C>A GRCh38
NC_000017.10:g.48263708C>A , CM000679.1:g.48263708C>A GRCh37
NC_000017.9:g.45618707C>A NCBI36
NG_007400.1:g.20293G>T , LRG_1:g.20293G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.3975G>T MANE Select NP_000079.2:p.Trp1325Cys
ENST00000225964.10:c.3975G>T MANE Select ENSP00000225964.6:p.Trp1325Cys
NM_000088.3:c.3975G>T , LRG_1t1:c.3975G>T NP_000079.2:p.Trp1325Cys
ENST00000225964.9:c.3975G>T ENSP00000225964.5:p.Trp1325Cys
ENST00000510710.3:n.644G>T
XM_005257058.3:c.3705G>T XP_005257115.2:p.Trp1235Cys
XM_005257058.4:c.3705G>T XP_005257115.2:p.Trp1235Cys
XM_005257059.3:c.3057G>T XP_005257116.2:p.Trp1019Cys
XM_005257059.4:c.3057G>T XP_005257116.2:p.Trp1019Cys
XM_011524341.1:c.3777G>T XP_011522643.1:p.Trp1259Cys