Canonical Allele Identifier: CA1883381868
Community Standard Title: NM_000093.5(COL5A1):c.3350G= (p.Gly1117=)
Gene: COL5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134806280G= , CM000671.2:g.134806280G= GRCh38
NC_000009.11:g.137698126G= , CM000671.1:g.137698126G= GRCh37
NC_000009.10:g.136837947G= NCBI36
NG_008030.1:g.169475G=

Transcript Alleles

HGVS Amino-acid Change
NM_000093.5:c.3350G= MANE Select NP_000084.3:p.Gly1117=
ENST00000371817.8:c.3350G= MANE Select ENSP00000360882.3:p.Gly1117=
NM_000093.4:c.3350G= NP_000084.3:p.Gly1117=
NM_001278074.1:c.3350G= NP_001265003.1:p.Gly1117=
ENST00000371817.7:c.3350G= ENSP00000360882.3:p.Gly1117=
ENST00000371820.4:c.3350G= ENSP00000360885.4:p.Gly1117=
ENST00000618395.4:c.3350G= ENSP00000481360.1:p.Gly1117=
XM_017014266.2:c.3350G= XP_016869755.1:p.Gly1117=
XR_001746183.1:n.3748G=
XR_929712.1:n.3752G=
XR_929713.1:n.3752G=