Canonical Allele Identifier: CA1883386794
Community Standard Title: NM_000093.5(COL5A1):c.4906G= (p.Ala1636=)
Gene: COL5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134824807G= , CM000671.2:g.134824807G= GRCh38
NC_000009.11:g.137716653G= , CM000671.1:g.137716653G= GRCh37
NC_000009.10:g.136856474G= NCBI36
NG_008030.1:g.188002G=

Transcript Alleles

HGVS Amino-acid Change
NM_000093.5:c.4906G= MANE Select NP_000084.3:p.Ala1636=
ENST00000371817.8:c.4906G= MANE Select ENSP00000360882.3:p.Ala1636=
NM_000093.4:c.4906G= NP_000084.3:p.Ala1636=
NM_001278074.1:c.4906G= NP_001265003.1:p.Ala1636=
NR_103451.2:n.71-4598C=
ENST00000371817.7:c.4906G= ENSP00000360882.3:p.Ala1636=
ENST00000371820.3:c.164G=
ENST00000371820.4:c.4906G= ENSP00000360885.4:p.Ala1636=
ENST00000460264.5:n.374G=
ENST00000465877.1:n.86G=
ENST00000618395.4:c.4906G= ENSP00000481360.1:p.Ala1636=
XM_017014266.2:c.4906G= XP_016869755.1:p.Ala1636=
XR_001746183.1:n.5304G=
XR_929712.1:n.5308G=
XR_929713.1:n.5308G=