Canonical Allele Identifier: CA467653374
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137642668C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134750822C>T , CM000671.2:g.134750822C>T GRCh38
NC_000009.11:g.137642668C>T , CM000671.1:g.137642668C>T GRCh37
NC_000009.10:g.136782489C>T NCBI36
NG_008030.1:g.114017C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371820.4:c.1602C>T ENSP00000360885.4:p.Ser534=
ENST00000371817.8:c.1602C>T MANE Select ENSP00000360882.3:p.Ser534=
ENST00000371817.7:c.1602C>T ENSP00000360882.3:p.Ser534=
ENST00000618395.4:c.1602C>T ENSP00000481360.1:p.Ser534=
NM_000093.4:c.1602C>T NP_000084.3:p.Ser534=
NM_001278074.1:c.1602C>T NP_001265003.1:p.Ser534=
XR_929712.1:n.2004C>T
XR_929713.1:n.2004C>T
XM_017014266.2:c.1602C>T XP_016869755.1:p.Ser534=
XR_001746183.1:n.2000C>T
NM_000093.5:c.1602C>T MANE Select NP_000084.3:p.Ser534=