Canonical Allele Identifier: CA467668295
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137734125G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134842279G>C , CM000671.2:g.134842279G>C GRCh38
NC_000009.11:g.137734125G>C , CM000671.1:g.137734125G>C GRCh37
NC_000009.10:g.136873946G>C NCBI36
NG_008030.1:g.205474G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371820.4:c.5493G>C ENSP00000360885.4:p.Val1831=
ENST00000371817.8:c.5493G>C MANE Select ENSP00000360882.3:p.Val1831=
ENST00000371817.7:c.5493G>C ENSP00000360882.3:p.Val1831=
ENST00000618395.4:c.5493G>C ENSP00000481360.1:p.Val1831=
NM_000093.4:c.5493G>C NP_000084.3:p.Val1831=
NM_001278074.1:c.5493G>C NP_001265003.1:p.Val1831=
NR_103451.2:n.71-22070C>G
NM_000093.5:c.5493G>C MANE Select NP_000084.3:p.Val1831=
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