Canonical Allele Identifier: CA375462087
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137734118T>A (hg19) chr9:g.134842272T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134842272T>A , CM000671.2:g.134842272T>A GRCh38
NC_000009.11:g.137734118T>A , CM000671.1:g.137734118T>A GRCh37
NC_000009.10:g.136873939T>A NCBI36
NG_008030.1:g.205467T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371820.4:c.5486T>A ENSP00000360885.4:p.Phe1829Tyr
ENST00000371817.8:c.5486T>A MANE Select ENSP00000360882.3:p.Phe1829Tyr
ENST00000371817.7:c.5486T>A ENSP00000360882.3:p.Phe1829Tyr
ENST00000618395.4:c.5486T>A ENSP00000481360.1:p.Phe1829Tyr
NM_000093.4:c.5486T>A NP_000084.3:p.Phe1829Tyr
NM_001278074.1:c.5486T>A NP_001265003.1:p.Phe1829Tyr
NR_103451.2:n.71-22063A>T
NM_000093.5:c.5486T>A MANE Select NP_000084.3:p.Phe1829Tyr
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