Canonical Allele Identifier: CA1883368872
Community Standard Title: NM_000093.5(COL5A1):c.4282C= (p.Gln1428=)
Gene: COL5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134818707C= , CM000671.2:g.134818707C= GRCh38
NC_000009.11:g.137710553C= , CM000671.1:g.137710553C= GRCh37
NC_000009.10:g.136850374C= NCBI36
NG_008030.1:g.181902C=

Transcript Alleles

HGVS Amino-acid Change
NM_000093.5:c.4282C= MANE Select NP_000084.3:p.Gln1428=
ENST00000371817.8:c.4282C= MANE Select ENSP00000360882.3:p.Gln1428=
NM_000093.4:c.4282C= NP_000084.3:p.Gln1428=
NM_001278074.1:c.4282C= NP_001265003.1:p.Gln1428=
ENST00000371817.7:c.4282C= ENSP00000360882.3:p.Gln1428=
ENST00000371820.4:c.4282C= ENSP00000360885.4:p.Gln1428=
ENST00000618395.4:c.4282C= ENSP00000481360.1:p.Gln1428=
XM_017014266.2:c.4282C= XP_016869755.1:p.Gln1428=
XR_001746183.1:n.4680C=
XR_929712.1:n.4684C=
XR_929713.1:n.4684C=