Canonical Allele Identifier: CA1883385828
Community Standard Title: NM_000093.5(COL5A1):c.3906+3G=
Gene: COL5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134814039G= , CM000671.2:g.134814039G= GRCh38
NC_000009.11:g.137705885G= , CM000671.1:g.137705885G= GRCh37
NC_000009.10:g.136845706G= NCBI36
NG_008030.1:g.177234G=

Transcript Alleles

HGVS Amino-acid Change
NM_000093.5:c.3906+3G= MANE Select NP_000084.3:n.3906+3G=
ENST00000371817.8:c.3906+3G= MANE Select ENSP00000360882.3:n.3906+3G=
NM_000093.4:c.3906+3G= NP_000084.3:n.3906+3G=
NM_001278074.1:c.3906+3G= NP_001265003.1:n.3906+3G=
ENST00000371817.7:c.3906+3G= ENSP00000360882.3:n.3906+3G=
ENST00000371820.4:c.3906+3G= ENSP00000360885.4:n.3906+3G=
ENST00000618395.4:c.3906+3G= ENSP00000481360.1:n.3906+3G=
XM_017014266.2:c.3906+3G= XP_016869755.1:n.3906+3G=
XR_001746183.1:n.4304+3G=
XR_929712.1:n.4308+3G=
XR_929713.1:n.4308+3G=