Canonical Allele Identifier: CA467668288
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137734116A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134842270A>T , CM000671.2:g.134842270A>T GRCh38
NC_000009.11:g.137734116A>T , CM000671.1:g.137734116A>T GRCh37
NC_000009.10:g.136873937A>T NCBI36
NG_008030.1:g.205465A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371820.4:c.5484A>T ENSP00000360885.4:p.Gly1828=
ENST00000371817.8:c.5484A>T MANE Select ENSP00000360882.3:p.Gly1828=
ENST00000371817.7:c.5484A>T ENSP00000360882.3:p.Gly1828=
ENST00000618395.4:c.5484A>T ENSP00000481360.1:p.Gly1828=
NM_000093.4:c.5484A>T NP_000084.3:p.Gly1828=
NM_001278074.1:c.5484A>T NP_001265003.1:p.Gly1828=
NR_103451.2:n.71-22061T>A
NM_000093.5:c.5484A>T MANE Select NP_000084.3:p.Gly1828=