Canonical Allele Identifier: CA467667209
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137726969C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134835123C>A , CM000671.2:g.134835123C>A GRCh38
NC_000009.11:g.137726969C>A , CM000671.1:g.137726969C>A GRCh37
NC_000009.10:g.136866790C>A NCBI36
NG_008030.1:g.198318C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371820.4:c.5289C>A ENSP00000360885.4:p.Ala1763=
ENST00000371817.8:c.5289C>A MANE Select ENSP00000360882.3:p.Ala1763=
ENST00000371817.7:c.5289C>A ENSP00000360882.3:p.Ala1763=
ENST00000371820.3:c.547C>A
ENST00000618395.4:c.5289C>A ENSP00000481360.1:p.Ala1763=
NM_000093.4:c.5289C>A NP_000084.3:p.Ala1763=
NM_001278074.1:c.5289C>A NP_001265003.1:p.Ala1763=
NR_103451.2:n.71-14914G>T
NM_000093.5:c.5289C>A MANE Select NP_000084.3:p.Ala1763=
Search 100 bp 5'
Search 100 bp 3'