Canonical Allele Identifier: CA364671401
Community Standard Title: NM_001851.6(COL9A1):c.460G>T (p.Val154Leu)
Gene: COL9A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.70294403C>A , CM000668.2:g.70294403C>A GRCh38
NC_000006.11:g.71004106C>A , CM000668.1:g.71004106C>A GRCh37
NC_000006.10:g.71060827C>A NCBI36
NG_011654.1:g.13681G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001851.6:c.460G>T MANE Select NP_001842.3:p.Val154Leu
ENST00000357250.11:c.460G>T MANE Select ENSP00000349790.6:p.Val154Leu
NM_001377291.1:c.460G>T NP_001364220.1:p.Val154Leu
NM_001851.4:c.460G>T NP_001842.3:p.Val154Leu
NM_001851.5:c.460G>T NP_001842.3:p.Val154Leu
ENST00000357250.10:c.460G>T ENSP00000349790.6:p.Val154Leu
ENST00000370496.3:c.460G>T ENSP00000359527.3:p.Val154Leu
XM_011535429.1:c.460G>T XP_011533731.1:p.Val154Leu
XM_011535429.3:c.460G>T XP_011533731.1:p.Val154Leu
XM_017010246.2:c.-12-78G>T XP_016865735.1:n.-12-78G>T