Canonical Allele Identifier: CA3882834
Community Standard Title: NM_001851.6(COL9A1):c.352C>T (p.Arg118Ter)
Gene: COL9A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.70294511G>A , CM000668.2:g.70294511G>A GRCh38
NC_000006.11:g.71004214G>A , CM000668.1:g.71004214G>A GRCh37
NC_000006.10:g.71060935G>A NCBI36
NG_011654.1:g.13573C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001851.6:c.352C>T MANE Select NP_001842.3:p.Arg118Ter
ENST00000357250.11:c.352C>T MANE Select ENSP00000349790.6:p.Arg118Ter
NM_001377291.1:c.352C>T NP_001364220.1:p.Arg118Ter
NM_001851.4:c.352C>T NP_001842.3:p.Arg118Ter
NM_001851.5:c.352C>T NP_001842.3:p.Arg118Ter
ENST00000357250.10:c.352C>T ENSP00000349790.6:p.Arg118Ter
ENST00000370496.3:c.352C>T ENSP00000359527.3:p.Arg118Ter
XM_011535429.1:c.352C>T XP_011533731.1:p.Arg118Ter
XM_011535429.3:c.352C>T XP_011533731.1:p.Arg118Ter
XM_017010246.2:c.-12-186C>T XP_016865735.1:n.-12-186C>T