Canonical Allele Identifier: CA5320190
Community Standard Title: NM_000093.5(COL5A1):c.4192G>A (p.Ala1398Thr)
Gene: COL5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134817793G>A , CM000671.2:g.134817793G>A GRCh38
NC_000009.11:g.137709639G>A , CM000671.1:g.137709639G>A GRCh37
NC_000009.10:g.136849460G>A NCBI36
NG_008030.1:g.180988G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000093.5:c.4192G>A MANE Select NP_000084.3:p.Ala1398Thr
ENST00000371817.8:c.4192G>A MANE Select ENSP00000360882.3:p.Ala1398Thr
NM_000093.4:c.4192G>A NP_000084.3:p.Ala1398Thr
NM_001278074.1:c.4192G>A NP_001265003.1:p.Ala1398Thr
ENST00000371817.7:c.4192G>A ENSP00000360882.3:p.Ala1398Thr
ENST00000371820.4:c.4192G>A ENSP00000360885.4:p.Ala1398Thr
ENST00000618395.4:c.4192G>A ENSP00000481360.1:p.Ala1398Thr
XM_017014266.2:c.4192G>A XP_016869755.1:p.Ala1398Thr
XR_001746183.1:n.4590G>A
XR_929712.1:n.4594G>A
XR_929713.1:n.4594G>A