Canonical Allele Identifier: CA375460369
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137726861G>C (hg19) chr9:g.134835015G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134835015G>C , CM000671.2:g.134835015G>C GRCh38
NC_000009.11:g.137726861G>C , CM000671.1:g.137726861G>C GRCh37
NC_000009.10:g.136866682G>C NCBI36
NG_008030.1:g.198210G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371820.4:c.5181G>C ENSP00000360885.4:p.Gln1727His
ENST00000371817.8:c.5181G>C MANE Select ENSP00000360882.3:p.Gln1727His
ENST00000371817.7:c.5181G>C ENSP00000360882.3:p.Gln1727His
ENST00000371820.3:c.439G>C
ENST00000618395.4:c.5181G>C ENSP00000481360.1:p.Gln1727His
NM_000093.4:c.5181G>C NP_000084.3:p.Gln1727His
NM_001278074.1:c.5181G>C NP_001265003.1:p.Gln1727His
NR_103451.2:n.71-14806C>G
XR_929712.1:n.5865G>C
XR_929713.1:n.5733G>C
NM_000093.5:c.5181G>C MANE Select NP_000084.3:p.Gln1727His
Search 100 bp 5'
Search 100 bp 3'