Canonical Allele Identifier: CA467652997
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137582879C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134691033C>G , CM000671.2:g.134691033C>G GRCh38
NC_000009.11:g.137582879C>G , CM000671.1:g.137582879C>G GRCh37
NC_000009.10:g.136722700C>G NCBI36
NG_008030.1:g.54228C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371820.4:c.231C>G ENSP00000360885.4:p.Val77=
ENST00000371817.8:c.231C>G MANE Select ENSP00000360882.3:p.Val77=
ENST00000371817.7:c.231C>G ENSP00000360882.3:p.Val77=
ENST00000464187.1:n.417C>G
ENST00000618395.4:c.231C>G ENSP00000481360.1:p.Val77=
NM_000093.4:c.231C>G NP_000084.3:p.Val77=
NM_001278074.1:c.231C>G NP_001265003.1:p.Val77=
XR_929712.1:n.633C>G
XR_929713.1:n.633C>G
XM_017014266.2:c.231C>G XP_016869755.1:p.Val77=
XR_001746183.1:n.629C>G
NM_000093.5:c.231C>G MANE Select NP_000084.3:p.Val77=