Canonical Allele Identifier: CA467667193
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137726966G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134835120G>A , CM000671.2:g.134835120G>A GRCh38
NC_000009.11:g.137726966G>A , CM000671.1:g.137726966G>A GRCh37
NC_000009.10:g.136866787G>A NCBI36
NG_008030.1:g.198315G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371820.4:c.5286G>A ENSP00000360885.4:p.Lys1762=
ENST00000371817.8:c.5286G>A MANE Select ENSP00000360882.3:p.Lys1762=
ENST00000371817.7:c.5286G>A ENSP00000360882.3:p.Lys1762=
ENST00000371820.3:c.544G>A
ENST00000618395.4:c.5286G>A ENSP00000481360.1:p.Lys1762=
NM_000093.4:c.5286G>A NP_000084.3:p.Lys1762=
NM_001278074.1:c.5286G>A NP_001265003.1:p.Lys1762=
NR_103451.2:n.71-14911C>T
NM_000093.5:c.5286G>A MANE Select NP_000084.3:p.Lys1762=